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EPM Events Calendar

Please find below details of forthcoming Pharmaceutical events from around the world.

You can sort them in date order, by location or by name.

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• Safety and Value: Critical Success Factors for Post-Approval Research
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• 2nd Successful eCTD Lifecycle Management
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• 2nd Successful eCTD Lifecycle Management
• analytica China
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• analytica China
• Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
• Pharmaceutical Production Batch Record Review
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• analytica China
• Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
• Pharmaceutical Production Batch Record Review
• Quality of Active Pharmaceutical Ingredients
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• Quality of Active Pharmaceutical Ingredients
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• Quality of Active Pharmaceutical Ingredients
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• CMC Regulatory Compliance for Biopharmaceuticals and Biologics
• Validation of Computer Systems
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• CMC Regulatory Compliance for Biopharmaceuticals and Biologics
• Validation of Computer Systems
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• CMC Regulatory Compliance for Biopharmaceuticals and Biologics
• Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
• Combating Counterfeit Drugs
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• Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
• Combating Counterfeit Drugs
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• Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
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• Adverse Drug Events – Reporting & Regulatory Requirements
• Design Control for Medical Device Professionals
• Writing Effective Standard Operating Procedures and Other Process Documents
• 1st Joint DIA/EMA Workshop on Statistical Methodology in Clinical R&D
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• Adverse Drug Events – Reporting & Regulatory Requirements
• Design Control for Medical Device Professionals
• Writing Effective Standard Operating Procedures and Other Process Documents
• 1st Joint DIA/EMA Workshop on Statistical Methodology in Clinical R&D
• Joint DIA/EFGCP Pharmacovigilance Audit and Inspection Workshop on Opportunities for Patient Safety
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• 1st Joint DIA/EMA Workshop on Statistical Methodology in Clinical R&D
• Joint DIA/EFGCP Pharmacovigilance Audit and Inspection Workshop on Opportunities for Patient Safety
• Design Validation, Verification, and Risk Analysis for Medical Device Professionals
• The Drug Development Process - From Discovery to Commercialization
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• Design Validation, Verification, and Risk Analysis for Medical Device Professionals
• The Drug Development Process - From Discovery to Commercialization
• Effective Document Management for Pharmaceutical, Biotech, & Medical Device Industries
• Global Approach to the Risk Management of Medicines
Date Town Country Event Title
23 Feb 2010 to 24 Feb 2010 Paris France Pharmapack
As an annual event, Pharmapack is the first platform for exchanges dedicated to packaging and drug delivery systems innovations for the pharmaceutical industry....read more
Event Website www.pharmapack.fr
23 Feb 2010 to 24 Feb 2010 Paris France BIOMEDevice Europe
BIOMEDevice is the first European event to focus on the development of the next generation of combination products. As drug delivery systems continue to evolve and the medical device, biopharmaceutical and pharmaceutical industries converge, BIOMEDev...read more
Event Website www.biomedevice-europe.com
23 Feb 2010 to 24 Feb 2010 Paris France BIOMEDevice Europe
BIOMEDevice is the first European event to focus on the development of the next generation of combination products. As drug delivery systems continue to evolve and the medical device, biopharmaceutical and pharmaceutical industries converge, BIOMEDev...read more
Event Website www.biomedevice-europe.com
7 Apr 2010 to 8 Apr 2010 Somerset USA Implementation of Effective & Compliant CAPA Programs
A Two-day interactive Workshop and Case Study Sessions on: Regulatory Requirements for CAPAs The importance of a Process Improvement Team in a strong CAPA program Global Harmonization Task Force- SG3 Common misconceptions about CAPAs Develop...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=capa0410nj
8 Apr 2010 to 9 Apr 2010 Dublin Ireland Project Management for Phase 1 & 2 Clinical Trials
Efficient and effective management of Phase 1 and 2 clinical trials can significantly impact the time, scope and budget for the development of a drug or device. Project managers must understand the development process and the key aspects of Phase 1 ...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=100&source=pe
8 Apr 2010 Palo Alto USA GMP auditor training for pharmaceutical companies
In this GMP auditor training for pharmaceutical companies you will learn what a GMP auditor should do and how to conduct an audit....read more
Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701627?channel=EPM
12 Apr 2010 to 13 Apr 2010 Dublin Ireland Project Management for the Phase 3 and LCM (Life Cycle Management) of the Drug Development Process
Speed to market is the key to driving product revenue. Managing the quality of the Phase 3 and 4 activities will impact project timing and budget and have a significant effect on the bottom line. Project managers must understand the late stage devel...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=101&source=pe
12 Apr 2010 to 13 Apr 2010 Berlin Germany Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
Complex processes yielding complex products such as biologics and biopharmaceuticals demand numerous, non-compendial, and sometimes complex, QC test methods to confirm manufacturing consistency and product quality. This course provides a comprehensi...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=096&source=pe
12 Apr 2010 to 14 Apr 2010 Berlin Germany Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
Course notes and interactive exercises address how to write effective correspondence and reports in support of the company’s activities. You will learn how to organize and deliver information for the intended audience. You will learn how to write cle...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=077&source=pe
13 Apr 2010 to 14 Apr 2010 Reading United Kingdom Qualified Person - Mathematics and Statistics
The study guide emphasises that QPs must have a knowledge of the practical application of basic statistical tools in pharmaceutical production and QA. This knowledge is essential in demonstrating the capability of processes or the acceptability of ma...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/qualifiedpersontrainingcourses/Pages/qualifiedperson.aspx
14 Apr 2010 to 15 Apr 2010 Montreal Canada GMP Chapter Effective Quality Assurance Auditing
Identify opportunities to improve your internal audit activity's ability to add value and improve operations - and develop actions to move forward on the path to quality This two-day "hands on" training course & workshops will address various topic...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=auditing0410mon
14 Apr 2010 to 16 Apr 2010 Berlin Germany CMC Regulatory Compliance for Biopharmaceuticals and Biologics
With the rapid development and constantly changing Chemistry, Manufacturing & Controls (CMC) landscape, it is more important than ever for a company to have an effective strategy to achieve CMC regulatory compliance. At each stage of drug deve...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=017&source=pe
14 Apr 2010 to 16 Apr 2010 Nice France Leigh White
The purpose of this training course is to provide Non-Biotechnologists with the basic theory to understand principles, techniques and the potentials of Biotechnology. Biotechnology combines disciplines such as Molecular Biology, Biochemistry, Chem...read more
Event Website http://www.management-forum.co.uk/gxp/eventid/1256
15 Apr 2010 to 16 Apr 2010 Berlin Germany Writing Effective Standard Operating Procedures and Other Process Documents
This course presents a comprehensive overview of process writing that the binding regulations require. There’s a tenet among regulatory bodies: “If you didn’t write it down, it didn’t happen,” and while the regulations tell companies what they need ...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=083&source=pe
15 Apr 2010 Webinar EU Technical infrastructure - striking the right balance to optimise compliance and value
In this webinar HOCHTIEF Facility Management will provide an overview of the key issues facing producers operating in highly controlled cGMP environments and tools that can be used to enhance performance. The webinar will set out a framework for look...read more
Event Website http://www.marketkey.co.uk/webinars/39/operational_excellence_in_your_pharmaceutical_manufacturing_operations.html
19 Apr 2010 to 21 Apr 2010 Reading UK Good Manufacturing Practice
An intensive course primarily aimed at key personel working in QA, QC, production, engineering and clinical trials, who wish to have a broader appreciation of GMP. It covers specific GMPs associated with different dosage forms, key facilities, the MH...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
19 Apr 2010 to 21 Apr 2010 Dublin Ireland cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
This course will provide the participant knowledge of current GMPs, how they are applied in the Bio/Pharmaceutical market today, and how they will be enforced in the future. Topics included are: * Impact of facility and equipment desi...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=095&source=pe
19 Apr 2010 to 21 Apr 2010 Berlin Germany QA/QC Strategy for Biopharmaceuticals and Biologics
While there are considerable similarities between biologics/biopharmaceuticals and chemically-synthesized drug products, many of the QA/QC issues and challenges are significantly different. Biology-based drug products are more complex products, deri...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=065&source=pe
19 Apr 2010 to 20 Apr 2010 Berlin Germany Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
If you didn’t write it down, it didn’t happen! This is the position of the FDA and most regulatory agencies internationally. Good documentation is vital for doing business in the regulated world from discovery through marketplace. It is also importa...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=027&source=pe
20 Apr 2010 to 22 Apr 2010 New York, NY USA INTERPHEX 2010
This global marketplace showcases the latest innovations and technological advancements occurring across the Pharmaceutical industry. INTERPHEX meets your needs and solves your issues – Increase productivity, increase product quality, maximize yields...read more
21 Apr 2010 to 23 Apr 2010 Tokyo Japan CPhI/ICSE/P-MEC/BioPh Japan 2010
CPhI Worldwide started in 1990 as an international convention on pharmaceutical ingredients and intermediates. The first CPhI Worldwide in 1990 attracted 250 visitors for 16 companies, while nowadays 24,000 industry professionals visit some 1.500 exh...read more
Event Website www.cphijapan.com
22 Apr 2010 Reading Uniited Kingdom Introduction to Microbiology
A course designed to give delegates background knowledge on the wide-ranging impact of mcirobiology on many aspects of pharmaceutical control. The course looks at the nature of micro-organisms, contamination sources and control, sterilisation and di...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
22 Apr 2010 to 23 Apr 2010 Dublin Ireland Pharmaceutical and Biopharmaceutical Quality Control Laboratories - A Regulatory Compliance Primer
This course is intended to give participants a thorough overview and practical understanding of Current Good Manufacturing Practices for laboratory compliance including: * General requirements for design and construction of analytical labor...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=097&source=pe
22 Apr 2010 to 23 Apr 2010 Berlin Germany Medical Devices - EU Directives, Guidance, CE Marking and ISO Standard Certifications
This is a two-day workshop focusing on understanding the requirements of the Medical Device Directives, their linkage to the EU Clinical Trial Directive and the requirements of CE Marking and ISO Certification on commercializing products. The course...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=092&source=pe
22 Apr 2010 to 23 Apr 2010 Berlin Germany Introduction to Effective Medical Writing
High-quality medical writing, which has a multi-million dollar impact on a company’s financial performance, can prevent the need for additional clinical trials which are often required because of unclear communication and poorly written documents. G...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=047&source=pe
22 Apr 2010 to 23 Apr 2010 London United Kingdom Leigh White
An inspection conducted by the US FDA is a very important milestone in any pharmaceutical company’s lifecycle. A successful inspection opens the door or retains access to one of the world’s most lucrative markets. When it is unsuccessful, the inspect...read more
Event Website http://www.management-forum.co.uk/gxp/eventid/1257
22 Apr 2010 Palo Alto USA Process Validation for Drugs and Biologics
In this Process Validation learn how to validate a manufacturing process and do it in a reasonable time....read more
Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701628?channel=EPM
26 Apr 2010 to 28 Apr 2010 London UK Optimising Clinical Development in Oncology
Through a series of interactive presentations and discussions, Pharma IQ’s Optimising Clinical Development in Oncology conference provides a unique platform for manufacturers to discuss practical, proven ideas to save time and money and ensure that c...read more
Event Website http://www.oncologysummit.co.uk/Event.aspx?id=251294&utm_source=DiaryListings&utm_medium=online&utm_campaign=DiaryListings&MAC=18515.001DL
26 Apr 2010 to 27 Apr 2010 Berlin Germany The EU Clinical Trial Directive
This course focuses on understanding the requirements of the new EU Clinical Trial Directive and the issues inherent in any new regulatory process. The course covers all relevant topics associated with the Directive, the reasons behind its introduct...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=030&source=pe
26 Apr 2010 to 27 Apr 2010 Dublin Ireland FDA Inspections of Clinical Data Systems
This course focuses on preparation for FDA systems inspections whether establishing a new program or seeking improvements in an ongoing quality initiative. The course provides practical information for improving presentation and substance of Clinical...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=034&source=pe
27 Apr 2010 to 29 Apr 2010 Nuremberg Germany TechnoPharm with POWTECH
Pharmaceuticals, food and cosmetics are among the most innovative industries throughout Europe. In view of rapidly growing markets, cleanroom technology places exacting demands on apparatus, plant and processes. TechnoPharm from 27–29 April 2010 is o...read more
27 Apr 2010 London UK Drug Metabolism Considerations in Drug Safety Assessment?
Professor Tom Baillie, Dean of the School of Pharmacy at the University of Washington will discuss how the FDA MIST and ICH M3(r2) guidelines encourage metabolism investigations earlier than ever in drug development...read more
Event Website http://www.quotientbioresearch.com/events/general/metabolism-c-14-enabled-early-drug-development
27 Apr 2010 to 28 Apr 2010 London UK Successful eCTD Lifecycle Management
This conference is designed to explore the planning, application and filing of eCTD submissions; highlighting the challenges that are faced and the latest regulatory guidelines. Case studies from key industry players as well as crucial insights from ...read more
Event Website http://www.ectdevent.com/Event.aspx?id=243414&utm_campaign=DiaryListing&utm_medium=weblisting&utm_source=genericdl&MAC=DLGENERIC
27 Apr 2010 to 28 Apr 2010 London UK PAT and Quality by Design for Biopharmaceuticals 2010
Pharma IQ is delighted to announce the inaugural PAT and Quality by Design for Biopharmaceuticals, being held in London on the 25th-26th May 2010. With PAT and Quality by Design techniques now established within the small molecules field the focus is...read more
Event Website http://www.biopatandqbd.com/Event.aspx?id=259248&utm_source=DiaryListings&utm_medium=online&utm_campaign=DiaryListings&MAC=18559.001DL
27 Apr 2010 to 28 Apr 2010 London United Kingdom Successful Implementation of Manufacturing Site Transfers - Considerations, Problems and Solutions - How to get it Right - A Practical Guide
This seminar will provide you with an overview of the regulatory, quality, logistics and project management consideration required for the efficient and effective transfer of both API and Drug Products between manufacturing sites, as well as the co-o...read more
Event Website http://www.management-forum.co.uk/gxp/eventid/1326
28 Apr 2010 to 29 Apr 2010 Berlin Germany European Filing & Registration Procedures
This course specifically focuses on agencies that control the regulatory process. The course will cover topics relating to pre-clinical and clinical requirements, as well as, addressing the structure of the regulatory agencies in the EU and individu...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=031&source=pe
10 May 2010 to 11 May 2010 Prague Czech Republic Fundamental Tools in Statistics for GMP Compliance
These two-day comprehensive hands on program will cover the following topics: Introduction and basic overview of Common Statistical Tools Fundamental Tools in Statistics Statistical Process Control - Pareto chart Control Charts Trending anal...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=statstools0510mid
10 May 2010 to 11 May 2010 Prague Czech Republic Fundamental Tools in Statistics for GMP Compliance
These two-day comprehensive hands on program will cover the following topics: Introduction and basic overview of Common Statistical Tools Fundamental Tools in Statistics Statistical Process Control - Pareto chart Control Charts Trendin...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=statstools0510mid
10 May 2010 to 11 May 2010 Prague Czech Republic Workshops on Investigating Out-of-Specification (OOS) Results
About the Workshop The essentials for conducting an investigation of an out-of specification result in a compliant, reliable, and timely manner include having a well-organized and understood process; having well-informed and well-trained analysts, s...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=oos0510czech
10 May 2010 to 11 May 2010 Prague Czech Republic Workshops on Investigating Out-of-Specification (OOS) Results
About the Workshop The essentials for conducting an investigation of an out-of specification result in a compliant, reliable, and timely manner include having a well-organized and understood process; having well-informed and well-trained analysts, s...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=oos0510czech
11 May 2010 to 12 May 2010 Reading United Kingdom Qualified Person - Foundation Module 2: Roles and Professional Duties
A Qualified Person (QP) must certify that each batch of medicinal product complies with its Marketing Authorisation or Product Specification File, GMP and certain other requirements. Their conduct overall must comply with the Code of Practice for QPs...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/qualifiedpersontrainingcourses/Pages/qualifiedperson.aspx
11 May 2010 London UK Species and Inter-species Dependent Metabolism in C-14 Enabled Drug Development
Professor Alan Rettie, Chairman, Department of Medicinal Chemistry, University of Washington, will explore the impact of inter-species differences on metabolism studies and the impact of inter-species genetic polymorphisms on metabolism....read more
Event Website http://www.quotientbioresearch.com/events/general/inter-and-intra-species-differences-drug-metabolism
11 May 2010 to 13 May 2010 Cincinnati, Ohio USA MM Live USA The Micro & Precision Manufacturing Event
MM Live USA is an event for manufacturers of precision micro components. The show is a global showcase for everything to do with the mass manufacture of small to micro precision parts, whether a company can make them to order or supply the machinery ...read more
Event Website www.mmliveusa.com
12 May 2010 to 14 May 2010 Bologna Italy Pharmintech
Pharmintech 2010 is an international showcase for the processing and packaging technology that serves the pharmaceutical, personal care, nutraceutical, and related industries. Worldwide buyers travel to Bologna, Italy to see what exhibitors from vari...read more
Event Website www.pharmintech.it
13 May 2010 Reading United Kingdom Good Manufacturing Practice
A one day course which examines why we have GMP, Its legal staus and the key GMP issues surrounding pharmaceutical manfucture such as documentation, training and facilities. An established, popular course aimed at any pharmaceutical professional who...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
17 May 2010 to 18 May 2010 Berlin Germany Practical Methods for Project Management
After completion of this course the attendee will have a strong understanding of the principles and practices of Project Management, including how to: * Work with the sponsor to start the project off in the right direction * Become a bett...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=060&source=pe
18 May 2010 to 19 May 2010 Reading United Kingdom Good Manufacturing Practice and Packagaing
A two-day course giving a detailed background into the complicated issues associated with pharmaceutical packaging. It examines all the key stages from artwork design, component suppliers through the packing process to final product release. It ide...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
18 May 2010 to 19 May 2010 St. Charles, Missouri United States Basics of Tablet Manufacturing and Troubleshooting
This Technical Training course takes a fundamental look at tablet manufacturing from design to compression. Learn about tablet design, tablet press set-up and troubleshooting, tooling options, rework, polishing, and inspection. This course is des...read more
Event Website http://natoli.com/Training/Technical-Training-Schedule.aspx
19 May 2010 to 20 May 2010 London UK GMP Auditor Training
Participants will learn about the key techniques and thought processes which may be used by auditors to maximize the benefits of each type of audit. These include planning and preparation, the audit team, structuring the audit, close out, CAPAs and ...read more
Event Website http://pharma-training-courses.com/gmp-auditor-training.html
19 May 2010 to 21 May 2010 Berlin Germany Root Cause Analysis for CAPA
Upon completion of this course, participants will have gained an understanding of the basic concepts involved in Root Cause Analysis and the tools used to conduct this activity. Participants will learn through experiential activities such as group d...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=069&source=pe
19 May 2010 to 20 May 2010 London UK Technology Transfer
This two-day interactive workshop is intended to provide an overview of the challenges that must be overcome in transferring technology and to highlight some proven techniques for overcoming those challenges. Some of the benefits to be derived fro...read more
Event Website http://www.pharma-training-courses.com/technology-transfer-for-pharmaceutical-products.html
19 May 2010 to 20 May 2010 Somerset USA Solid Dosage Production in cGMP Manufacturing
An Interactive and Comprehensive One & Half-Day Course On: Formulation and Production cGMPs Pharmaceutical Mixing Materials for Direct Compression Formulation with Binders, Fillers, Glidants, Lubricants, and Disintegrants Screening and Sie...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=manufacturing0510nj
19 May 2010 to 20 May 2010 Somerset USA Residual Solvents Testing: How to Apply USP <467>
At the end of the course, the students will have an understanding of the regulatory requirements regarding residual solvents, will have practical information about how to apply the specifications and when testing is required, will be familiar with th...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=residual0510nj
20 May 2010 Reading United Kingdom Good Distribution Practie (GDP)
An intensive course intended to evaluate Good Distribution Practices (GDP) as required by Directive 2001/83/EC, Directive 2004/27/EC, EU Guidelines on Good Distribution of Medicinal Products for Human Use 94/C 63/03 and the new requirements included ...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
21 May 2010 to 21 May 2010 Beckenham UK How to Audit API Manufacturers
This one-day seminar is aimed at QA staff in drug products manufacturers and especially their QPs who have specific responsibilities under directive 2004/27/EV. QPs are required to declare that the active materials used in each of their products hav...read more
Event Website http://www.pharma-training-courses.com/how-to-audit-api-manufacturers.html
24 May 2010 to 25 May 2010 Berlin Germany Clinical Trial Design for Medical Devices
The objective of this course is to provide an overview of the preparation, design and management aspects of clinical trials for medical devices. Upon completion of this course, attendees will have an understanding of the unique challenges faced in c...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=014&source=pe
24 May 2010 to 25 May 2010 Berlin Germany Overview of FDA Regulatory Compliance for Medical Devices
This course is specifically focused on the law, regulations and policies set down by the FDA for the manufacture of medical devices. It will provide each attendee with the background and knowledge necessary to understand the organization, structure ...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=020&source=pe
25 May 2010 to 27 May 2010 Birmingham UK Total Processing and Packaging 2010
As a leading UK integrated processing & packaging exhibition, Total Processing & Packaging 2010 showcases production line solutions from beginning to end. Attracting key professionals from major sectors including food & drink, pharmaceutical, c...read more
Event Website www.totalexhibition.com
25 May 2010 to 26 May 2010 Miami USA Dissolution Testing in Pharmaceutical Analysis
A TWO-DAY COMPREHENSIVE and INTERACTIVE CONFERENCE, with CASE STUDIES, WORKSHOP and EXHIBITION addressing: Regulatory Requirements for Dissolution Testing Change in Criteria for USP Dissolution Performance Verification Test Role of Dissolutio...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=dissolution0510mia
26 May 2010 to 27 May 2010 Berlin Germany Process Validation for Medical Devices
The purpose of this course is to provide an introduction to the fundamentals of process validation, explaining how, when, where and why you should validate. Learn how to comply with FDA regulations for validation protocols and determine the format an...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=089&source=pe
26 May 2010 to 27 May 2010 Nice France THE EU PHARMACEUTICAL DOSSIER – CTD MODULES 2.3 and 3
The conference will provide a wide-ranging, up-to-date coverage of the pharmaceutical issues that underpin a successful marketing authorisation application. In a carefully-structured programme, delegates will learn about the key components of the EU...read more
Event Website http://www.management-forum.co.uk/gxp/eventid/1329
26 May 2010 to 27 May 2010 Montreal Canada What to expect and how to prepare for FDA Inspection
A Two-day comprehensive and interactive program with case studies on: Authority for FDA Inspections Legal scope and limits of FDA inspections Current FDA Positioning / ‘Threats’ Types of Inspection How to get a quick Assessment of a Company ...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=fdapreapprov0510mon
27 May 2010 to 27 May 2010 Jersey City USA Contamination Control Strategies
This one full day Comprehensive training will address the following topics: Sources and quantities of microbial contamination Using the QSIT approach assess microbiological contamination and their sources Biofilms Objectionable microorganis...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=contamin0510nj
1 Jun 2010 to 4 Jun 2010 Paris France Forum labo
Noroit will be presenting their new safety cabinets, Cabinets for robots protections, PCR cabinets All the team will be there.. www.noroitlabo.com...read more
Event Website http://www.forumlabo.com/
2 Jun 2010 to 4 Jun 2010 Pudong-Shanghai China CPhI/ICSE/P-MEC/BioPh China 2010
CPhI Worldwide started in 1990 as an international convention on pharmaceutical ingredients and intermediates. The first CPhI Worldwide in 1990 attracted 250 visitors for 16 companies, while nowadays 24,000 industry professionals visit some 1.500 exh...read more
Event Website www.cphi-china.com
7 Jun 2010 to 11 Jun 2010 Oxford United Kingdom Quality Management Systems Lead Auditor Training (IRCA Ref A17129)
An intensive five day course focused on ISO9001 and the specific GMP standards that have been developed for the supply of packaging and excipient materials to the pharmaceutical industry. ISO9001 is covered in detail and this will enable pharmaceuti...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
7 Jun 2010 to 9 Jun 2010 Reading United Kingdom Formulation and Porcessing Part 1
The Qualified Person should be the company expert in the formulation and processing of medicinal products they are asked to certify. This five day (2 part) module provides basic formulation principles, including preformulation studies, bioavailabilit...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/qualifiedpersontrainingcourses/Pages/qualifiedperson.aspx
7 Jun 2010 to 8 Jun 2010 Prague Czech Republic Common Sense Computer Validation for Regulated Systems
Course Abstract: This course teaches a practical approach to computer validation based on requirements from around the world for companies subject to GMP, GLP, GCP, and 21 CFR Part 11 regulations. More than 20 years of validation experience is con...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=comsys0610czech
8 Jun 2010 to 9 Jun 2010 Montreal Canada Quality Risk Management
A Two-day interactive course with workshops, case studies and interactive exercises on: Risk Management Basics The ISO 31000 global risk management process model Current Risk Management initiatives (ICH, FDA, ISO etc.) and regulatory expectati...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=qualityrisk0610mon
8 Jun 2010 Manchester United Kingdom Thermo Fisher Scientific UK Summer Symposia
Thermo Fisher Scientific is pleased to announce that it is hosting two free-of-charge summer symposia to present the latest instrumentation and application developments in chromatography, bulk elemental analysis, life sciences mass spectrometry, trac...read more
Event Website http://www.thermoscientific.com/summersymposium.
10 Jun 2010 London United Kingdom Thermo Fisher Scientific UK Summer Symposia
Thermo Fisher Scientific is pleased to announce that it is hosting two free-of-charge summer symposia to present the latest instrumentation and application developments in chromatography, bulk elemental analysis, life sciences mass spectrometry, trac...read more
Event Website http://www.thermoscientific.com/summersymposium
15 Jun 2010 to 16 Jun 2010 Reading United Kingdom Responsible Person
A one-day course covering an evaluation of the key roles and responsibilities of the Responsible Person (RP) and Deputy RP in relation to Directive 2001/83/EC, Directive 2004/27/EC, EU Guidelines on Good Distribution of Medicinal Products for Human U...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
15 Jun 2010 to 16 Jun 2010 London United Kingdom PHARMACEUTICAL PACKAGING
Further information will follow shortly. Please contact ellen.walker@management-forum.co.uk for further information in the meantime. ...read more
Event Website http://www.management-forum.co.uk/gxp/eventid/1325
15 Jun 2010 to 16 Jun 2010 Boston USA Implementation of Effective & Compliant CAPA Programs
A Two-day interactive Workshop and Case Study Sessions on: Regulatory Requirements for CAPAs Understanding of CAPA System Elements of a Corrective Action Program Common misconceptions about CAPAs The importance of a Process Improvement Team ...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=capa0610bo
15 Jun 2010 to 16 Jun 2010 Boston USA Best Practices for science and compliance in: Pharmaceutical Microbiology
Microbiological contamination of products and processes continues to be a major concern to the industry and its regulators. The potential impact of such contamination can be catastrophic. Put simply, microbial contamination can kill your patients and...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=microbiology0610ma
17 Jun 2010 Reading United Kingdom Documentation
Documentation is the cornerstone of any company's Quality Management System and is an essential GMP requirement. It is critical that anyone dealing with GMP documents and documentation systems understand the regulatory requirements and adopts best p...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
21 Jun 2010 to 23 Jun 2010 Frankfurt Germany The 9th Annual Biological Production Forum 2010
This is the event focusing on both upstream and downstream processing for biological manufacturing, production and cGMP specialists. Over the course of this 3 day event, you will take part in a mixture of networking and conference session featuring t...read more
Event Website http://www.biologicalproduction.com/
22 Jun 2010 Reading United Kingdom Environmental Monitoring
A one-day course that addresses environmental monitoring for the manufacturing of both sterile and non-sterile products. It looks at the legislation and guidance available, techniques employed to monitor pharmaceutical environments, data trending an...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
22 Jun 2010 Boston, MA USA Accelerating Early Stage Development and the FDA’s Critical Path Initiative
PharmaNet Development Group is pleased to announce that it is hosting two complimentary symposia and roundtable discussions entitled “Accelerating Early Stage Development and the FDA’s Critical Path Initiative.” The symposia will include timely t...read more
23 Jun 2010 Princeton, New Jersey USA Accelerating Early Stage Development and the FDA’s Critical Path Initiative
PharmaNet Development Group is pleased to announce that it is hosting two complimentary symposia and roundtable discussions entitled “Accelerating Early Stage Development and the FDA’s Critical Path Initiative.” The symposia will include timely t...read more
29 Jun 2010 to 1 Jul 2010 Nice France IMPURITIES, IMPURITIES, IMPURITIES - 10th Annual Update - Chemical, Pharmaceutical, Pharmacopoeial, Biological, Microbiological, Licensing, GMP and other Regulatory Matters
With additional focus on: EU GUIDELINES AND UPDATED GUIDANCE ON GENOTOXIC IMPURITIES AND ON SPECIFICATION SETTING FOR THESE IMPURITIES This conference takes a look at impurities from numerous perspectives with presentations on avoidance, detectio...read more
Event Website http://www.management-forum.co.uk/gxp/eventid/1200
30 Jun 2010 to 1 Jul 2010 Canary Wharf United Kingdom Clinically Relevant Drug Transporters
Improve your Understanding and Modelling of Drug Transporters to Better Predict Drug-Drug Interactions, Enhance Interaction Study Efficiency and Increase Drug Efficacy...read more
Event Website www.drugtransporters.com
5 Jul 2010 to 7 Jul 2010 Reading United Kingdom Qualified Person - Formulation and Processing Part 2
The Qualified Person should be the company expert in the formulation and processing of medicinal products they are asked to certify. This five day (2 part) module provides basic formulation principles, including preformulation studies, bioavailabilit...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/qualifiedpersontrainingcourses/Pages/qualifiedperson.aspx
8 Jul 2010 to 9 Jul 2010 London United Kingdom MICROBIOLOGICAL ISSUES IN PHARMACEUTICAL PRODUCTION AND CONTROL
Microbiological issues play a central part in the production and control of manufactured items. An understanding of the significance of microbiological data is essential for those who need to interpret and act upon results. This seminar will give...read more
Event Website http://www.management-forum.co.uk/gxp/eventid/1327
13 Jul 2010 to 14 Jul 2010 Reading United Kingdom Internal Auditing
A highly interactive and practical training course aimed at people working in the pharmaceutical industry who are about to start auditing or those who already audit but have no formal training. It provides an introduction to the guideline for Qualit...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
15 Jul 2010 Reading United Kingdom Good Manufacturing Practice in the Laboratory
A course specifically designed for laboratory staff who have unique, additional requirements laid down in GMP. The course concentrates on Chapter 6 (QC and Good Control Laboratory Practice0 of the EU Guide to GMP. It also covers the role of Pharmac...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
20 Jul 2010 Reading United Kingdom Qualified Person - Biotechnology Issues
The QP needs to understand the quality issues associated with the manufacture of biopharmaceuticals. Whilst the other modules cover biotechnology products alongside other product types, based around the study guide, this workshop is designed to pull ...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/qualifiedpersontrainingcourses/Pages/qualifiedperson.aspx
20 Jul 2010 to 22 Jul 2010 St. Charles, Missouri United States Fundamentals of Blending, Compression and Coating of Tablets and Tooling
Attend this course and maximize your knowledge of tablet manufacturing, tooling care and tablet presses while identifying and addressing common industry pitfalls. This course is designed for individuals in the tablet manufacturing industry that d...read more
Event Website http://natoli.com/Training/Technical-Training-Schedule.aspx
20 Jul 2010 to 21 Jul 2010 Calgary Canada Solid Dosage Production in cGMP Manufacturing
An Interactive and Comprehensive One & Half-Day Course On: Formulation and Production cGMPs Pharmaceutical Mixing Materials for Direct Compression Formulation with Binders, Fillers, Glidants, Lubricants, and Disintegrants Screening and Sievi...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=manufacturing0710cal
22 Jul 2010 to 22 Jul 2010 Palo Alto USA Key Factors to Write an Effective Standard Operating Procedure (SOP)
In this Effective Standard Operating Procedure (SOP) training learn how to develop a comprehensive, consistent SOP. The critical elements of a SOP which is easier to understand follow and review by operating personnel....read more
Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701674?channel=EPM
29 Jul 2010 London UK Free Webinar: The Seven Keys for Effective Solid Dosage Manufacturing
The best manufacturing companies follow "key steps" that set them apart from the typical solid dosage manufacturing company. - Learn what techniques they consider to be the "best" and how to implement them - Discover ‘the seven keys’ to becoming a...read more
Event Website http://www.wtgwebinar.com/webinar/the-seven-keys-for-effective-solid-dosage-manufacturing/113
9 Aug 2010 to 11 Aug 2010 St. Charles, Missouri United States Pharmaceutical Tablet Technology
Designed to train a wide range of individuals involved with the design, formulation, manufacture, quality control, quality assurance and bioavailability of pharmaceutical tablets. Tablet press operators, tablet press maintenance technicians, gran...read more
Event Website http://natoli.com/Training/Technical-Training-Schedule.aspx
10 Aug 2010 to 11 Aug 2010 Washington DC USA Auditing and Qualifying API Suppliers
A Two-Day Comprehensive and Interactive Course with Workshops on: Why audit API Manufacturers? The roles of secondary manufacturers Background to ICHQ7 How to create a successful and efficient API supplier qualification program Qualification ...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=audit0610wash
11 Aug 2010 to 11 Aug 2010 Palo Alto USA Streamline Documentation System in Pharmaceutical Laboratory
This laboratory documentation training Webinar will discuss the GMP requirements on laboratory records and how to streamline documentation system....read more
Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701677?channel=EPM
17 Aug 2010 to 19 Aug 2010 Buenos Aires Argentina CPhI/ICSE/P-MEC/BioPh South America 2010
CPhI Worldwide started in 1990 as an international convention on pharmaceutical ingredients and intermediates. The first CPhI Worldwide in 1990 attracted 250 visitors for 16 companies, while nowadays 24,000 industry professionals visit some 1.500 exh...read more
Event Website www.cphi-sa.com
17 Aug 2010 to 18 Aug 2010 Montreal Canada The International API GMP Guidance: ICH Q7 Implementation and Application
Addressing Issues on Regulatory Requirements, Guidelines and Practical Approaches to API’s Manufacturing This comprehensive 2-day program was developed along with FDA to train both regulatory (FDA) and Industry personnel. It was written by members o...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=ichq0810mon
17 Aug 2010 to 18 Aug 2010 Montreal Canada Process Validation Workshops for pharmaceutical
2-Day Process Validation Workshops on: Manufacturing Process Validation Planning – The Risk Analysis Failure Modes and Effects Analysis Design of Experiments for Manufacturing Processes Simple Design of Experiments for a Tablet Compression Proces...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=ichq0810mon
19 Aug 2010 to 20 Aug 2010 Mumbai India NDDS 2010: Novel Drug Delivery Systems India
NDDS India 2010 is a two-day strategic conference which will help you to uncover the key challenges and opportunities that will enable you to drive the potential of new drug delivery systems in your organisation....read more
Event Website http://www.ndds-india.com/?utm_campaign=EVENTCALENDAR&utm_medium=EVENTLISTING&utm_source=EPMMAGAZINECOM
26 Aug 2010 to 27 Aug 2010 Mumbai India SCM Pharma India 2010
SCM Pharma India 2010 is the only Pharmaceutical Supply Chain Management conference designed specifically for the Indian market....read more
Event Website http://www.scmpharma-india.com/?utm_campaign=EVENTCALENDAR&utm_medium=EVENTLISTING&utm_source=EPMMAGAZINECOM
30 Aug 2010 to 30 Aug 2010 Palo Alto,CA United States 2010 Changes to the EU Variation Rules, Classifications and Submittal Requirements
This European Regulatory webinar is designed to provide an overview on the changes to the variation rules, classifications and filing requirements for all active pharmaceutical, biologics and orphan drug licenses in the EU....read more
Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701739?channel=EPM
31 Aug 2010 to 31 Aug 2010 Palo Alto,CA USA Streamline Documentation System in Pharmaceutical Laboratory
This laboratory documentation training Webinar will discuss the GMP requirements on laboratory records and how to streamline documentation system....read more
Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701677?channel=EPM
2 Sep 2010 London UK Optimizing Overall Manufacturing System Performance: Cell Culture Supplementation
Opportunities to optimize manufacturing system performance can be found through cell culture supplementation. Specifically in animal-free cell culture supplements. InVitria, a company specializing in cell culture media supplements, is leading the w...read more
Event Website http://www.wtgwebinar.com/webinar/optimizing-overall-manufacturing-system-performance:-cell-culture-supplementation-/111
2 Sep 2010 to 2 Sep 2010 35-43 Lincoln’s Inn Field, London, WC2A 3PE UK Safety and Value: Critical Success Factors for Post-Approval Research
Key note speakers from companies such as PharmaNet, Eisai Europe and Abacus International will all be presenting during the event Featured topics include: • Strategic Post-Approval Research Planning • The Evolving Post-Approval Regulatory Envi...read more
8 Sep 2010 to 8 Sep 2010 Palo Alto,CA USA Engineering and Laboratory Mythology with Water System
This water systems webinar training will discuss the myths surrounding microbial monitoring and control approaches and alert you to the pitfalls of believing these myths which could cause over-confidence in a system’s design for microbial control or ...read more
Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701477?channel=EPM
9 Sep 2010 to 9 Sep 2010 Palo Alto,CA USA Key Factors to Write an Effective Standard Operating Procedure (SOP)
In this Effective Standard Operating Procedure (SOP) training learn how to develop a comprehensive, consistent SOP. The critical elements of a SOP which is easier to understand follow and review by operating personnel....read more
Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701674?channel=EPM
14 Sep 2010 to 16 Sep 2010 Reading United Kingdom Qualified Person - Packaging
The QP needs to fully understand the challenges and risks involved in packaging operations in the Pharmaceutical Industry. A significant percentage of all product related complaints and recalls are related to packaging. This course closely examines t...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/qualifiedpersontrainingcourses/Pages/qualifiedperson.aspx
14 Sep 2010 to 15 Sep 2010 Prague Czech republic 2nd Successful eCTD Lifecycle Management
Pharma IQ is delighted to announce the 2nd Successful eCTD Lifecycle Management conference, being held in Prague on the 14th and 15th of September 2010. With eCTD submissions taken a firm hold in the US and Japan, they are now making their mark i...read more
Event Website www.ectdevent.com/prague
14 Sep 2010 Macclesfield UK Technical Visit to AstraZeneca
The visit to AstraZeneca Macclesfield will provide an overview of two sterile plants that manufacture the product Zoladex, which is used in the treatment of breast and prostate cancer. Zoladex was first manufactured in 1987 and due to the fact that t...read more
Event Website www.filtsoc.org
14 Sep 2010 to 14 Sep 2010 Palo Alto,CA USA The role of Analytical Program to Support Drug Development Process
This drug development process training Webinar will give an overview of drug development process, the regulatory requirements and the analytical technology used for pharmaceutical analysis supporting R & D....read more
Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701667?channel=EPM
15 Sep 2010 to 17 Sep 2010 Shanghai China analytica China
analytica China, the analytica China Conference and the exhibition portfolio for analysis, laboratory technology, diagnostics and biotechnology, address one of the industry's most important growth markets in Asia, i.e. China. The exhibition is held e...read more
Event Website www.analytica.de
16 Sep 2010 to 17 Sep 2010 Dublin Ireland Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
Complex processes yielding complex products such as biologics and biopharmaceuticals demand numerous, non-compendial, and sometimes complex, QC test methods to confirm manufacturing consistency and product quality. This course provides a comprehensi...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=096&source=pe
16 Sep 2010 to 17 Sep 2010 Berlin Germany Pharmaceutical Production Batch Record Review
Efficient and effective batch record reviews provide pharmaceutical companies with two strategies. First, reviews are key to maintaining control of your firm’s operations, eliminating any guesswork and aiding in the resolution of atypical occurrence...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=058&source=pe
17 Sep 2010 to 19 Sep 2010 Mumbai India Quality of Active Pharmaceutical Ingredients
This conference is organized in cooperation with World Health Organization (WHO), The European Directorate for the Quality of Medicine & Health Care (EDQM) and Drug Information Association (DIA). The major focus of this conference will be on the curr...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23922&eventType=Meeting
17 Sep 2010 to 17 Sep 2010 Palo Alto,CA USA Forced Degradation Studies/ Biologics Stability Programs for Biopharmaceuticals
This training on Forced Degradation study on a Protein Therapeutic will discuss on the Forced Degradation Studies required for Well Characterized Protein Therapeutic products and how to leverage forced degradation results to design stability studies ...read more
Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701748?channel=EPM
20 Sep 2010 to 22 Sep 2010 Dublin Ireland CMC Regulatory Compliance for Biopharmaceuticals and Biologics
With the rapid development and constantly changing Chemistry, Manufacturing & Controls (CMC) landscape, it is more important than ever for a company to have an effective strategy to achieve CMC regulatory compliance. At each stage of drug develop...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=017&source=pe
20 Sep 2010 to 21 Sep 2010 Dublin Ireland Validation of Computer Systems
This course focuses on developing and implementing regulated computer systems with an appropriate level of documented evidence to satisfy FDA expectations. The course targets deliverable document content and how to avoid rework and unnecessary expen...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=081&source=pe
21 Sep 2010 to 22 Sep 2010 Reading United Kingdom External Auditing
A two-day course covering the skills and processes necessary to perform effective external audits and follows the processes described in ISO 19011 – the international standard for auditing. The course focuses on the specific standards used by extern...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
21 Sep 2010 to 22 Sep 2010 Philadelphia USA The International API GMP Guidance: ICH Q7 Implementation and Application
Addressing Issues on Regulatory Requirements, Guidelines and Practical Approaches to API’s Manufacturing This comprehensive 2-day program was developed along with FDA to train both regulatory (FDA) and Industry personnel. It was written by members o...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=ichq0910ph
22 Sep 2010 to 22 Sep 2010 Palo Alto USA Stability Program to support Shipping and Distribution of Drug Products
Learn key factors affecting shipping and distribution of product and the stability studies that should be done to support shipping and distribution....read more
Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701678?channel=EPM
22 Sep 2010 to 24 Sep 2010 Dublin Ireland Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
This course focuses on developing and implementing regulated computer systems with an appropriate level of documented evidence to satisfy FDA expectations. The course targets deliverable document content and how to avoid rework and unnecessary expen...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=077&source=pe
22 Sep 2010 to 23 Sep 2010 Mississauga Canada Combating Counterfeit Drugs
Recent examples of counterfeit pharmaceuticals (case studies) Regulatory oversight and enforcement: examples from selected countries in Mekong region...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=counterfeit0910to
22 Sep 2010 to 22 Sep 2010 Palo Alto,CA USA Stability Program to support Shipping and Distribution of Drug Products
Learn key factors affecting shipping and distribution of product and the stability studies that should be done to support shipping and distribution....read more
Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701678?channel=EPM
22 Sep 2010 to 22 Sep 2010 Palo Alto,CA USA The Hero of Manufacturing Contamination Control -- The Microbiology Lab
This webinar on Contamination Control will discuss, how the micro lab can be more effectively utilized to prevent or head off microbial contamination issues as well as effectively resolve problems like recurring micro failures, investigations, and in...read more
Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701478?channel=EPM
27 Sep 2010 to 28 Sep 2010 Dublin Ireland Adverse Drug Events – Reporting & Regulatory Requirements
This course will provide participants with an understanding of drug safety at the investigational stage and during the marketing phase. Adverse event identification and reporting requirements will be addressed, as well as FDA, EMEA, Health Canada and...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=002&source=pe
27 Sep 2010 to 28 Sep 2010 Dublin Ireland Design Control for Medical Device Professionals
This continually updated course covers current FDA regulatory compliance with respect to developing medical devices. A focus will be placed on basic regulation and the FDA's supplemental guidelines. Among the topics to be discussed are: context o...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=024&source=pe
27 Sep 2010 to 28 Sep 2010 Dublin Ireland Writing Effective Standard Operating Procedures and Other Process Documents
This course presents a comprehensive overview of process writing that the binding regulations require. There’s a tenet among regulatory bodies: “If you didn’t write it down, it didn’t happen,” and while the regulations tell companies what they need ...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=083&source=pe
27 Sep 2010 to 29 Sep 2010 Vienna Austria 1st Joint DIA/EMA Workshop on Statistical Methodology in Clinical R&D
This 2 ½ day event is the first joint DIA/EMA workshop on statistical methodology in clinical research and development. In 2009 a Biostatistics Drafting Group was formed at the EMA, comprising 10 statisticians from National Competent Authorities. The...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=22706&eventType=Meeting
28 Sep 2010 to 29 Sep 2010 London UK Joint DIA/EFGCP Pharmacovigilance Audit and Inspection Workshop on Opportunities for Patient Safety
Organised by EFGCP in partnership with DIA The EFGCP Children’s Medicines Working Party and DIA Europe are pleased to announce their second joint paediatric conference. Traditional paediatric meetings of both societies in the past and the joint me...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23618&eventType=Meeting
29 Sep 2010 to 30 Sep 2010 Dublin Ireland Design Validation, Verification, and Risk Analysis for Medical Device Professionals
This course covers current FDA regulatory compliance with respect to developing medical devices. Focus will be placed on relevant aspects of FDA regulation to V&V and Risk Analysis and the FDA's supplemental guidelines. An ISO perspective is offere...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=118&source=pe
29 Sep 2010 to 1 Oct 2010 Dublin Ireland The Drug Development Process - From Discovery to Commercialization
The drug development process involves a series of lengthy steps that determine the degree of success for every drug brought to the market. Decisions made throughout the process affect every aspect of future development and impact heavily on commercia...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=025&source=pe
30 Sep 2010 to 1 Oct 2010 Dublin Ireland Effective Document Management for Pharmaceutical, Biotech, & Medical Device Industries
If you didn’t write it down, it didn’t happen! This is the position of the FDA and most regulatory agencies internationally. Good documentation is vital for doing business in the regulated world from discovery through marketplace. It is also importa...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=027&source=pe
30 Sep 2010 to 1 Oct 2010 Washington DC USA Global Approach to the Risk Management of Medicines
Join Authorities, Global Regulators, Industry Representatives, and Marketing Application Holders for an Interactive Discussion of RMPS. This conference will teach you how to identify and organize essential components of RMPs as they apply to medic...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23726&eventType=Meeting
1 Oct 2010 London UK Joint DIA/EFGCP Pharmacovigilance Audit and Inspection - Opportunities for Patient Safety
The aim of this workshop is: • To provide a neutral platform for regulators and industry to jointly review experience from pharmacovigilance audits and inspections across national boundaries • To increase the common understanding of the role of p...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23321&eventType=Meeting
1 Oct 2010 to 1 Oct 2010 Palo Alto,CA USA GMPs in Biopharmaceutical Development Laboratories
This GMP webinar training on Biopharmaceutical lab provides the attendee with an overview of the GMPs as they pertain to early phase development labs. This course satisfies the annual mandatory training required for personnel employed in GMP laborato...read more
Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701749?channel=EPM
3 Oct 2010 to 6 Oct 2010 Aix-en-Provence France Innovation in Drug Delivery: From Preformulation to Development
2nd conference on "Innovation in Drug Delivery: From Preformulation to Development through Innovative Evaluation Process."
Plenary lecture, oral presentations, technical sessions and posters.
Organizers: APGI (International Society of Dr...read more
Event Website http://www.apgi.org/2ndInnovDrugDeliv.htm
5 Oct 2010 to 6 Oct 2010 Reading United Kingdom Qualified Person - Microbiology
The QP needs an understanding of the microbiological control of pharmaceutical products. Delegates will discuss the main types and sources of micro-organisms and the issues associated with them in relation to sterile and non-sterile pharmaceutical pr...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/qualifiedpersontrainingcourses/Pages/qualifiedperson.aspx
5 Oct 2010 to 7 Oct 2010 Paris France CPhI/ICSE/P-MEC/BioPh Worldwide 2010
CPhI Worldwide started in 1990 as an international convention on pharmaceutical ingredients and intermediates. The first CPhI Worldwide in 1990 attracted 250 visitors for 16 companies, while nowadays 24,000 industry professionals visit some 1.500 exh...read more
Event Website www.cphi.com
5 Oct 2010 to 6 Oct 2010 Dublin Ireland The EU Clinical Trial Directive
This course focuses on understanding the requirements of the new EU Clinical Trial Directive and the issues inherent in any new regulatory process. The course covers all relevant topics associated with the Directive, the reasons behind its introduct...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=030&source=pe
5 Oct 2010 to 6 Oct 2010 Philadelphia USA Analysis of Metal Impurities According to Proposed USP Chapters
The United State Pharmacopoeia, USP has significantly changed the way metal analysis in drugs and dietary supplements. In January 2010 USP proposed three new chapters on elemental impurities (<232>, <2232>, and <233>) with new requirements for limit...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=analysis1010ph
5 Oct 2010 to 6 Oct 2010 Washington DC USA Development of Type 2 Diabetes Mellitus Drugs: State of the Art Cardiovascular Safety Assessments
CALL FOR ABSTRACTS Please submit all abstracts via email to Rachel Minnick, Program Developer Rachel.Minnick@diahome.org All abstracts must be received by September 8, 2010. Please provide all information in PowerPoint or MSWord format Co-sponsor...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23808&eventType=Meeting
6 Oct 2010 to 8 Oct 2010 Prague Czech Republic Comprehensive Training on European Regulatory Affairs including Different Registration Procedures and Variations: Expert Overview
The ‘Comprehensive Training on European Regulatory Affairs including different Registration Procedures and Variations: Expert Overview’ training course is a key course developed by DIA in Europe. This course provides a comprehensive description and d...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23851&eventType=Training%20Course
7 Oct 2010 to 8 Oct 2010 Dublin Ireland European Filing & Registration Procedures
This course specifically focuses on agencies that control the regulatory process. The course will cover topics relating to pre-clinical and clinical requirements, as well as, addressing the structure of the regulatory agencies in the EU and individu...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=031&source=pe
11 Oct 2010 to 12 Oct 2010 Dublin Ireland Medical Devices - EU Directives, Guidance, CE Marking and ISO Standard Certifications
This is a two-day workshop focusing on understanding the requirements of the Medical Device Directives, their linkage to the EU Clinical Trial Directive and the requirements of CE Marking and ISO Certification on commercializing products. The course...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=092&source=pe
11 Oct 2010 to 13 Oct 2010 Lisbon Portugal 4th Annual Clinical Forum 2010
Topics: Clinical Data Management/eClinical • Clinical Operations • Clinical Research • Peri- and Post-Approval Studies • Drug Safety and Risk Management • Quality Assurance • Clinical Endpoints • e-Technology and Validation • Medical Informat...read more
Event Website http://www.diahome.org/DIAHome/FlagshipMeetings/Home.aspx?meetingID=22350
12 Oct 2010 to 13 Oct 2010 Reading United Kingdom Internal Auditing
A highly interactive and practical training course aimed at people working in the pharmaceutical industry who are about to start auditing or those who already audit but have no formal training. It provides an introduction to the guideline for Qualit...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
12 Oct 2010 to 13 Oct 2010 Chester UK Filter Testing 5 International Conference, Exhibition and Short Course
The Filtration Society's Filter Testing bi-annual international conference and exhibition is one of the most attended events promoted by the Society and this year is no exception. The Filtration Society invites you to register for the one-day interna...read more
Event Website www.filtsoc.org
12 Oct 2010 to 13 Oct 2010 Bethesda USA Advancing Pediatric Research in the US
Join Pediatric Research Experts to Share Solutions to the Challenges Involved in Constructing and Conducting Global Pediatric Programs. Over the past three years industry has been busily climbing the steep learning curve of the EU Pediatric Legisl...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23614&eventType=Meeting
13 Oct 2010 to 14 Oct 2010 Bethesda USA Maternal and Pediatric Drug Safety Symposium
Join Leaders from Industry, Academia, CDC, FDA, EMA, and WHO to Discuss Emerging Topics in Maternal and Pediatric Drug Safety. Maternal and pediatric drug safety is becoming increasingly important areas in the life cycle of medical compounds. Rece...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23874&eventType=Meeting
13 Oct 2010 to 14 Oct 2010 Bethesda USA Early Drug Development: Navigating the Treacherous Rapids
Take Your Place at the Project Team Table and Contribute Toward Successfully Bringing Your Compound to a Decision Point. This dynamic, interactive, small molecule-focused workshop will teach you strategies to address the key issues facing project ...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23646&eventType=Meeting
13 Oct 2010 to 14 Oct 2010 National Harbor USA Investing in Biomedical Informatics for Drug Development and Health Care
his is the age of opportunity for health care! There is now so much health care data available that when it is aggregated, analyzed, mined and visualized it can provide the information needed to enable evidence-based, cost-effective, better health ca...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23256&eventType=Meeting
14 Oct 2010 to 14 Oct 2010 London United Kingdom THE ROLE OF THE RESPONSIBLE PERSON
INTRODUCTION Learn how to operate Good Distribution Standards under the Guidance of the UK MHRA Healthcare Regulations by following the Orange Guide. WHO SHOULD ATTEND This training course is aimed at: RPs / QPs, Directors, Heads and Manager...read more
Event Website http://www.management-forum.co.uk/gxp/eventid/1328
14 Oct 2010 to 15 Oct 2010 Rockville USA Partnerships to Advance Patient Recruitment and Retention in Clinical Research
Recruiting adequate numbers of clinical trial participants has always been difficult across diverse populations particularly in women, children, ethnic minorities and the aging sub-group populations. It is well-known and scientifically documented tha...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=22727&eventType=Meeting
18 Oct 2010 to 20 Oct 2010 Beijing China Joint DIA-ACT Study Director Workshop
Although this workshop is directed towards early-career toxicologists and related professional in the CRO industry, this course would be valuable to a broad range of nonclinical, clinical, management and regulatory personnel in pharmaceutical, medica...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23939&eventType=Meeting
19 Oct 2010 Reading United Kingdom Good Distribution Practice (GDP)
An intensive course intended to evaluate Good Distribution Practices (GDP) as required by Directive 2001/83/EC, Directive 2004/27/EC, EU Guidelines on Good Distribution of Medicinal Products for Human Use 94/C 63/03 and the new requirements included ...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
19 Oct 2010 to 20 Oct 2010 Coventry UK TCT Live 2010
Software & Technology for Product Development & Manufacturing TCT Live is the only UK event focused on providing solutions for reducing time-to-market. The exclusive focus on Rapid Product Development and Additive Manufacturing technologies sta...read more
Event Website www.tctshow.com
19 Oct 2010 to 20 Oct 2010 Coventry UK MM Live 2010
The Micro & Precision Manufacturing Event MM Live is an event for manufacturers of precision micro components. The show is a global showcase for everything to do with the mass manufacture of small to micro precision parts, whether a company ca...read more
Event Website www.micro-show.com
19 Oct 2010 to 21 Oct 2010 London United Kingdom Global Discovery Outsourcing and Collaborations Forum
Pharma IQ is proud to announce Global Discovery Outsourcing and Collaborations Forum, held in London on the 20th – 21st October 2010....read more
Event Website www.globaldiscoverycollaborations.com
20 Oct 2010 Reading United Kingdom Documentation
Documentation is the cornerstone of any company's Quality Management System and is an essential GMP requirement. It is critical that anyone dealing with GMP documents and documentation systems understand the regulatory requirements and adopts best p...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
21 Oct 2010 Reading United Kingdom Good Manufacturing Practice
A one day course examining why we have GMP, its legal status and the key GMp issues surrounding pharmaceutical manufacture such as documentation, training and facilities. An established, popular course aimed at any pharmaceutical professional who wi...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
23 Oct 2010 to 26 Oct 2010 Bangalore India 5th Annual Conference on Drug Discovery and Clinical Development Meeting the Challenges of Next Generation R&D: Enhancing Efficiency, Effectiveness and Innovation
Conference Topics: • Drug Discovery • Regulatory Aff airs • Early / Pre-Clinical Development • Clinical Operations • Quality Assurance and Compliance • Biologics and Vaccines • Pharmacovigilance and Drug Safety • Clinical Data Management, Bio...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23796&eventType=Meeting
25 Oct 2010 to 26 Oct 2010 Berlin Germany Best Practices for an Effective Cleaning Validation Program
This course provides practical guidance on cleaning validation regulatory compliance, in conjunction with, risk-based, reasonable and informed decision making and activity planning. The program will describe the requirements for establishing an effe...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=007&source=pe
25 Oct 2010 to 26 Oct 2010 Nice France 4th European Cardiac Safety Conference
Key Topics • The future of thorough QT assessment - Where do we go from here • Cardiovascular safety of oncology and biological pharmaceutical products • Cardiovascular safety beyond the QT interval - Drug effect on other ECG indices • Drug effec...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23320&eventType=Meeting
26 Oct 2010 to 27 Oct 2010 Reading United Kingdom Qualified Person - Analysis and Testing
The sampling and testing of materials does not by itself assure product quality. It must be part of a comprehensive ‘Quality Management System’, including QA and GMP, which must be correctly implemented and controlled. This module includes GCLP, inte...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/qualifiedpersontrainingcourses/Pages/qualifiedperson.aspx
26 Oct 2010 to 27 Oct 2010 Bethesda USA Tomorrow's Project Manager: Evolving Competencies for Biopharmaceutical Professionals
Address leading issues for the project management community, engage in discussions with leading project management experts, and discover competency model elements suitable for best practices. Where do you think pharmaceutical project management is...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23877&eventType=Meeting
26 Oct 2010 to 27 Oct 2010 Bethesda USA Ensuring Quality and Balancing Risks for Multiregional Clinical Trials: Statistical, Clinical, Regulatory, and Ethical Factors
The conference will provide discussions, experts and case studies addressing ethical, regulatory, operational, statistical, and clinical considerations of MRCTs, including: • Access to medicines and post-trial care • Ethical considerations • Intel...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23615&eventType=Meeting
27 Oct 2010 to 28 Oct 2010 Berlin Germany Process Validation for Drugs and Biologics
Process validation is not a curse invented by regulators and pushed onto a company by QA staff. Instead, it is a legal requirement in the pharmaceutical industry. The concept of process validation is recognition that quality cannot be tested into t...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=049&source=pe
27 Oct 2010 to 29 Oct 2010 San Diego USA The 9th Annual Electronic Submissions Conference: Working Together Towards a Global Strategy
The focus of this year’s meeting will be on developing and implementing an electronic submission strategy that will accommodate submission to one or many countries, including discussion of true simultaneous submission to regions. Tutorials: Octo...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23785&eventType=Meeting
28 Oct 2010 to 29 Oct 2010 Tokyo Japan 7th DIA Japan Annual Meeting
his conference aims to contribute to the further advancement of international clinical development by deepening the mutual understanding among those working in the pharmaceutical industry, academia and regulatory authorities. Event Code: 1030...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23312&eventType=Meeting
1 Nov 2010 to 5 Nov 2010 Oxford United Kingdom Quality Management Systems Lead Auditor Training (IRCA Ref A17129)
An intensive five day course focused on ISO9001 and the specific GMP standards that have been developed for the supply of packaging and excipient materials to the pharmaceutical industry. ISO9001 is covered in detail and this will enable pharmaceuti...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
2 Nov 2010 to 3 Nov 2010 Reading United Kingdom Responsible Person
A one-day course covering an evaluation of the key roles and responsibilities of the Responsible Person (RP) and Deputy RP in relation to Directive 2001/83/EC, Directive 2004/27/EC, EU Guidelines on Good Distribution of Medicinal Products for Human U...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
2 Nov 2010 to 3 Nov 2010 Somerset, NJ USA Cold Chain & Logistics Management
Preliminary Outline An Important Two-Day Conference with Interactive Exercise and Case Studies on: Regulatory changes and guidance expected in 2010 New Regulations on Storage, Handling and Distribution of Drug Samples & Mail-Order Drugs Extrapola...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=coldchain1110nj
2 Nov 2010 to 3 Nov 2010 Berlin Germany Preparation of FDA Submissions (INDs, NDAs, BLAs, ANDAs, Post-Approval Supplements) and Communicating with the FDA
This course will give participants the background and history of the US Food and Drug Administration (FDA) as a basis for the strategic planning of submitting INDs, NDAs, BLAs, ANDAs, and post-approval supplements. Each item of these submissions wi...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=085&source=pe
2 Nov 2010 to 3 Nov 2010 Berlin Germany Selecting and Managing CRO's
This course will provide the attendees with all the specific methodology and management techniques to successfully outsource pharmaceutical programs that are completed on time, within budget, and most importantly completed with a high level of qualit...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=086&source=pe
3 Nov 2010 Paris France Future Direction for Orphan Drugs in Europe
This 1st DIA conference on Orphan Drugs will reflect on the experience gained in the first 10 years of the European Orphan Medicinal Products (OMP) Regulation. It will review current developments in orphan drug research, look at points of collaborati...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23718&eventType=Meeting
4 Nov 2010 to 5 Nov 2010 Berlin Germany Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Processing Responsibilities
This course provides attendees with an understanding of the role DMFs play in the FDA's regulatory approval process for drugs and biologics. The course will take participants through a step-by-step process of DMF preparation and explain the types of...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=026&source=pe
4 Nov 2010 to 5 Nov 2010 Berlin Germany Stability Programs for Product Shelf Life - From Development to Approval
This continually updated course covers current FDA regulatory requirements and ICH guidelines as applied to designing stability programs from the early stages of product development all the way to approval. Among the topics to be discussed will be: ...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=072&source=pe
4 Nov 2010 to 5 Nov 2010 Ottawa Canada DIA’s 8th Annual Canadian Meeting: Fostering Innovation and Access to Drugs
TUTORIALS Wednesday, November 3 Preregistration required. Primer on Reimbursement An Overview of Signal Detection: See It, Analyze It, Deal with It The program will highlight information on improving efficiency in the running of clinical tria...read more
Event Website http://www.diahome.org/DIAHome/FlagshipMeetings/Home.aspx?meetingID=23405
4 Nov 2010 to 5 Nov 2010 Paris France 2nd Health Technology Assessment (HTA) Conference
This conference will bring together all stakeholders: from regulators to governments, from national competent authorities to the European Medicines Agency in London and from industry, payers and – the ultimate beneficiary of a successfully functionin...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23719&eventType=Meeting
4 Nov 2010 to 5 Nov 2010 Ottawa Canada DIA’s 8th Annual Canadian Meeting: Fostering Innovation and Access to Drugs
The program will highlight information on improving efficiency in the running of clinical trials; discussion of streamlining federal and provincial regulatory and formulary approvals; and advice on strategies to overcome obstacles. TUTORIALS Wednes...read more
Event Website http://www.diahome.org/DIAHOME/Education/MeetingEventRegistration.aspx?productID=23405&eventType=Meeting
4 Nov 2010 to 5 Nov 2010 Lansdowne USA DIA/FDA Orphan Drug Designation Workshop
Registration is limited (maximum of 3 persons per organization) and is accepted on a first-come, first-served basis. Registration closes October 27, 2010; on-site registration will not be available for this workshop. Over two full days, FDA sta...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23774&eventType=Meeting
9 Nov 2010 to 10 Nov 2010 Reading United Kingdom Good Manufacturing Practice and Packaging
A two-day course giving a detailed background into the complicated issues associated with pharmaceutical packaging. It examines all the key stages from artwork design, component suppliers through the packing process to final product release. It ide...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
9 Nov 2010 to 10 Nov 2010 Bethesda MD Sustaining Clinical Trial Disclosure
Conference: November 9-10, 2010 Preconference Workshop: November 8, 2010 • What Are the Connections Between HL7 and Clinical Trial Disclosure? Interact with Speakers from Industry and Regulatory and Government Agencies to Explore Global Perspecti...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23783&eventType=Meeting
9 Nov 2010 Zurich Switzerland Conference on Drug & Device Combination Products – Finding the Right Regulatory Strategy
This one-day conference will provide delegates with an understanding of the regulatory framework and highlight the challenges developing combination products. It will focus on the differences between device and pharma regulations and will provide ex...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23319&eventType=Meeting
10 Nov 2010 to 12 Nov 2010 Dublin Ireland The CTD/eCTD: Building the Marketing Application throughout Clinical Development
The guidance on marketing applications for drugs and biologics, known as the Common Technical Document (CTD), was finalized by the International Conference on Harmonization (ICH) in 2003. Today the CTD format is mandatory for paper-based marketing a...read more
Event Website http://www.cfpie.com/showitem.aspx?productid=078&source=pe
10 Nov 2010 to 12 Nov 2010 Sao Paulo Brazil 7th Latin American Congress of Clinical Research: Harmonization and the Future of Drug Development in Latin America
This three-day congress will include two pre-congress courses and a two-day conference focusing on both the global and regional aspects of clinical research. Registration is being handled by Managing Eventos. To register, please use the following ...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23627&eventType=Meeting
16 Nov 2010 to 18 Nov 2010 Reading United Kingdom Qualified Person - Foundation Module 3: Quality Management Systems
It is a fundamental requirement of GMP that organisations design and implement a Quality Management System (QMS) that is appropriate for their activities, is fully documented and monitored to ensure effectiveness. Without an effective QMS the QP cann...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/qualifiedpersontrainingcourses/Pages/qualifiedperson.aspx
18 Nov 2010 to 19 Nov 2010 Washington, DC USA Combating Counterfeit Drugs
Recent examples of counterfeit pharmaceuticals (case studies) Regulatory oversight and enforcement: examples from selected countries in Mekong region...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=counterfeit0910to
18 Nov 2010 to 19 Nov 2010 Washington, DC USA Combating Counterfeit Medicines
Combating pharmaceutical crime over the internet – Enforcement and public awareness. Anti-counterfeiting enforcement programs in the US. Building an effective in-house anti-counterfeiting program, and more......read more
Event Website http://www.ipacanada.com/viewcourse.php?id=counterfeit1110wash
23 Nov 2010 to 25 Nov 2010 Reading UK Good Manufacturing Practice
An intensive course primarily aimed at key personnel working in QA, QC, production, engineering and clinical trials, who wish to have a broader appreciation of GMP. It covers specific GMPs associated with different dosage forms, key facilities, the ...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
26 Nov 2010 London UK European Medicines Agency - ENCePP Information Day
The European Network of Centres for Pharmacoepidemiology and Pharmacovigilance (ENCePP) is a project led by the European Medicines Agency (EMA) to bring together the available expertise and research experience in the fields of Pharmacoepidemiology an...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=24003&eventType=Meeting
29 Nov 2010 to 30 Nov 2010 London UK 2nd Joint DIA/ European Medicines Agency Innovation Forum: Is the EU Regulatory Framework Ready?
The 2nd Innovation forum will provide an opportunity to address the progress of innovative medicines in legal, organisational and technical aspects of the pharmaceutical framework in Europe. It will address the implementation of the EMA/CHMP think-ta...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=22643&eventType=Meeting
29 Nov 2010 to 30 Nov 2010 London UK 2nd Joint DIA/ European Medicines Agency Innovation Forum: Is the EU Regulatory Framework Ready?
The 2nd Innovation forum will provide an opportunity to address the progress of innovative medicines in legal, organisational and technical aspects of the pharmaceutical framework in Europe. It will address the implementation of the EMA/CHMP think-ta...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=22643&eventType=Meeting
30 Nov 2010 to 2 Dec 2010 Berlin Germany World Drug Manufacturing
Increasing innovation and reducing costs across global operations. World Drug Manufacturing 2010 will focus on industry challenges occurring throughout small molecule and biologic manufacturing. The industry is facing pressure to reduce costs, to...read more
Event Website www.wdmsummit.com
30 Nov 2010 to 30 Nov 2010 Palo Alto,CA USA Why and How - Verification of Compendial Methods - USP <1226>
This verification of Compendial methods webinar training will discuss the requirements of USP <1226>, what are FDA expectations related to method verification....read more
Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701752?channel=EPM
1 Dec 2010 to 3 Dec 2010 Nice France 11th Conference on European Electronic Document Management
In an evolutionary environment, it seems that every time one overcomes a hurdle one discovers a whole new world to conquer. Similarly, in EDM we are discovering new frontiers. While on the regulatory submissions front, CTD and eCTD are now well known...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23224&eventType=Meeting
2 Dec 2010 Reading United Kingdom Introduction to Microbiology
A course designed to give delegates background knowledge on the wide-ranging impact of mcirobiology on many aspects of pharmaceutical control. The course looks at the nature of micro-organisms, contamination sources and control, sterilisation and di...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/Pages/training.aspx
2 Dec 2010 to 3 Dec 2010 Somerset, NJ USA Cold Chain & Logistics Management
Regulatory changes and guidance expected in 2010 New Regulations on Storage, Handling and Distribution of Drug Samples & Mail-Order Drugs Extrapolating Future Regulatory Requirements In-line with Cold Chain Trends Harmonized Guidance for the Stora...read more
Event Website http://www.ipacanada.com/viewcourse.php?id=coldchain1110nj
7 Dec 2010 to 8 Dec 2010 London United Kingdom Innovation in Clinical Design, Analysis and Reporting
Pharma IQ’s inaugural Innovation in Clinical Design, Analysis and Reporting conference will help to open up this area to debate, facilitate discussion between like-minded professionals within the field, presenting industry professionals with a forum ...read more
Event Website www.clinicalreporting.co.uk/Calendar
7 Dec 2010 to 9 Dec 2010 Washington DC USA US and International Prescription Drug Labeling Comparisons and Important Updates
Join Regulatory Authorities from Different Regions to Discuss Key Labeling Requirements, Recommendations, Trends, and New Developments. This conference will discuss issues commonly encountered by industry in an effort to advance understanding of l...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=24058&eventType=Meeting
8 Dec 2010 Reading United Kingdom Qualified Person - Investigational Medicinal Products
The QP needs to be aware of the different requirements between commercial and clinical trial operations. This is one day course examines EU legislation and GMP issues, many of which are unique, associated with Investigational Medicinal Products (IMPs...read more
Event Website http://www.rssl.com/services/pharmaceuticalandhealthcare/training/qualifiedpersontrainingcourses/Pages/qualifiedperson.aspx
19 Dec 2010 to 20 Dec 2010 London UK Next-Generation DNA Sequencing
Today’s Next-Generation DNA Sequencing systems are opening novel fields and applications in biology studies and medical research. At the Pharma IQ Next-Generation DNA Sequencing conference January 18-20 in London, you will share study and tech...read more
Event Website http://www.dnaevent.com/Event.aspx?id=234810&utm_campaign=DiaryListings&utm_medium=online&utm_source=DiaryListings&MAC=18267.001DL
7 Feb 2011 to 9 Feb 2011 Washington DC USA CMC Workshop: Translating Science into Successful Regulatory Submissions
Co-sponsored by the American Association of Pharmaceutical Scientists. Discuss Challenging Topics Facing the Pharmaceutical and Biopharmaceutical Communities from Development, Implementation, and Regulatory Submissions Perspectives. This CMC work...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23878&eventType=Meeting
8 Feb 2011 to 10 Feb 2011 Cologne Germany HuLST Expo
HuLST Expo - A global event for testing professionals, engineers and technicians Supporting the food and beverage, biotech, medical and pharmaceutical industries, the new HuLST (Human. Life. Science. Test) Expo will be held at the Koelnmesse. Co...read more
Event Website www.hulst-expo.com
14 Feb 2011 to 17 Feb 2011 National Harbor USA Electronic Document Management 2011: The Intersection of Data, Documents and Submissions
ver the past 23 years, the DIA EDM Conference has served as a forum for the discussion of emerging standards and the processes for the creation, submission and retention of regulatory information. This year’s program has been enhanced to provide a mo...read more
Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=23833&eventType=Meeting
22 Mar 2011 to 24 Mar 2011 Wiesbaden Germany FILTECH 2011
FILTECH is the largest special interest Event world-wide devoted entirely to filtration and separation technology. FILTECH is a must for all those concerned with designing, improving, purchasing, selling or researching filtration and separation equip...read more
Event Website http://www.filtech.de/
27 Sep 2011 to 29 Sep 2011 Birmingham UK INTERPLAS 2011 - The International Forum for the British Plastics Industry
Interplas is the UK's leading triennial plastics exhibition. For almost 60 years Interplas has successfully represented the plastic processing community in the UK and the 2011 exhibition is set to continue this success. The show floor will incorporat...read more
Event Website www.britishplasticsshow.com


 

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