European Pharmaceutical Manufacturer, the pharmaceutical supply chain for ingredients, equipment, contract services

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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Date	Town	Country	Event Title
7 Feb 2012 to 7 Feb 2012	Palo Alto	United States	Solutions for Addressing Fungal and Bacterial Spore Outbreaks in Pharmaceutical, Biotech, and Medical Device Operations
This webinar on addressing fungal and bacterial spore outbreaks will discuss case studies on excursion investigations and show how facility design, personnel practices and cleaning and disinfection effect excursion investigations....read more Event Website www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701766?channel=epmevents

7 Feb 2012 to 7 Feb 2012	Palo Alto	United States	Medical Device Regulations and Law in the US, EU and Canada
This 3-hr training will discuss medical device regulations and law in the US, Europe and Canada. It is designed to help the audience with their global compliance and regulatory intelligence, which is necessary to streamline the regulatory process in ...read more Event Website www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702200?channel=epmevents

7 Feb 2012 to 7 Feb 2012	Palo Alto	United States	Prepare for Tougher U.S. FDA cGMP Compliance Audits
This FDA cGMP training webinar will discuss US FDA’s approach to cGMP Audits and expectations from companies. It will also evaluate chief concern areas of cGMP compliance audit and anticipatory emphasis changes as per new regulatory climate....read more Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701432?channel=epmevents

8 Feb 2012 to 8 Feb 2012	Palo Alto	United States	Medical Device Process Validation - Statistical Considerations
This Process Validation training will look at the underlying statistical concepts to perform an effective process validation. The webinar examine elements of the FDA regulations for process validation (21 CFR §820.75) as well as the corresponding req...read more Event Website www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701630?channel=epmevents

9 Feb 2012 to 9 Feb 2012	Palo Alto	United States	Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina)
This 4-hr Latin America Regulatory compliance requirements training/webinar will cover topics relating to pre-clinical and clinical requirements, as well as, addressing the structure of the regulatory agencies in Latin America....read more Event Website www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702038?channel=epmevents

9 Feb 2012 to 9 Feb 2012	Palo Alto	United States	Purposeful Water and Steam System Validation – Not Just A Regulatory Requirement
This Water system validation training will guide you how validation should be customized to your particular water system design and maintenance practices, what operational elements should be included in the microbial testing during validation and whi...read more Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701358?channel=epmevents

10 Feb 2012 to 11 Feb 2012	Ahmedabad	India	CMC: Converting Science in to Regulatory Submission
Chemistry, Manufacturing and Controls (CMC) is one of the three areas that health authorities consider for the review and approval of drug applications. Effective CMC strategies and execution may reduce regulatory burden, enable shorter review times,...read more Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=29002&eventType=Meeting

14 Feb 2012 to 14 Feb 2012	Palo Alto	United States	FDA’s Current Thinking for Industry cGMPs for Phase 1 INDs
This US FDA draft guidance documentation webinar/ training will give an insider’s insight into the new guidance and regulation and discuss the rationale for such. The US FDA has issued a draft guidance document outlining a suggested approach to co...read more Event Website www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=700155?channel=epmevents

15 Feb 2012 to 16 Feb 2012	PARIS	FRANCE	Pharmapack Europe 2012
First European congress-exhibition dedicated to packaging technologies and delivery systems for drugs and medical products, Pharmapack Europe 2012 will gather over2800 visitors come from 50 countries and 260 exhibitors. Building on the success of th...read more Event Website www.pharmapack.fr

15 Feb 2012 to 15 Feb 2012	Palo Alto	United States	Environmental Monitoring and Contamination Control Plan
This 90-minute cleanroom contamination control training will review the common mistakes that people make in cleanrooms that lead to contamination, show how to develop a successful contamination control program and discuss ways to improve your facilit...read more Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702209?channel=epmevents

16 Feb 2012 to 16 Feb 2012	Palo Alto	United States	Complaint Handling in Compliance with FDA and ISO Regulations
This training will show how you can handle customer complaints in compliance with FDA and ISO Regulations. We will discuss the best ways to document customer feedback, what constitutes a complaint, what do with "non-complaint" feedback, and how to in...read more Event Website www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=700986?channel=epmevents

21 Feb 2012 to 21 Feb 2012	Palo Alto	United States	Design History Files, Device Master Records, Device History Records, and Technical Files / Design Dossiers -- Differences and Similarities
This webinar will examine in detail the U.S. FDA and EU MDD requirements for DHFs, DMRs, DHRs, and TF/DDs -- their commonalities and their differences. Why Should You Attend: Global companies must meet different product design documentation for...read more Event Website www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701898?channel=epmevents

23 Feb 2012 to 25 Feb 2012	Shanghai	China	The 2nd Clinical Project Management Training Course
With the success of the first Clinical Project Management (CPM) Training in 2011, DIA China will conduct the second CPM training on Feb. 23-25, 2012 in Shanghai. This 3-day training course is designed to meet the increasing demands for knowledge a...read more Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=28894&eventType=Training%20Course

23 Feb 2012 to 23 Feb 2012	Palo Alto	United States	Submission Documentation for Sterilization Process Validation - A Comprehensive View of Content for an Approvable CMC Section
In this sterility assurance documentation webinar, you will learn specifically what information is required in sterility assurance documentation for injectable drug products and how to present it in CTD format. ...read more Event Website www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701926?channel=epmevents

23 Feb 2012 to 23 Feb 2012	Palo Alto	United States	Understanding Design Controls for Medical Devices
This webinar will cover the basics of design controls for medical devices, and provide recommendations for implementation of a compliant design control system....read more Event Website www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701285?channel=epmevents

23 Feb 2012 to 23 Feb 2012	Palo Alto	United States	Navigating the Japan Regulatory and Clinical Trial Environment; Conducting Clinical Studies in Japan
This Japan Regulatory and Clinical Trial Requirements training will cover Japan Regulatory Agency Structure and Responsibilities, its review process for decision-making and approval, requirements for clinical trials in Japan and the procedures for co...read more Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702170?channel=epmevents

27 Feb 2012 to 29 Feb 2012	Washington, DC	USA	MICROBIOLOGY in Quality Control Laboratories
Regulatory Guidelines: FDA, EU, EMEA, MHRA, IMB ... Review of Some of the Typical Microbiological Tests Harmonization of Microbial Methods for Non-sterile Products - Practical Challenge Efficacy of Antimicrobial Preservation - USP, EP, JP, PCPC (F...read more Event Website http://ipacanada.com/microbiology-conference/

28 Feb 2012 to 29 Feb 2012	Zurich	Switzerland	ProcureCon Pharma
Find out at Procurecon Pharma 2012, a brand new pharmaceutical procurement conference focusing on the strategic issues and challenges facing senior pharmaceutical sourcing professionals. This two-day pharmaceutical sourcing conference will be a forum...read more Event Website www.ProcureCon-Pharma.com

28 Feb 2012 to 29 Feb 2012	Zurich	Switzerland	ProcureCon Pharma 2012
Find out at Procurecon Pharma 2012, an exciting new strategic sourcing conference for the pharma procurement community. Hear best practice case studies, challenges faced and lessons learnt from leading biopharma industry opinion formers and walk away...read more Event Website http://www.wbresearch.com/procureconpharma/ ?utm_campaign=European Pharmaceutical Manufacturer&utm_medium=Listing&utm_source=Media Partner&utm_content=Homepage&MAC=20777.001_epm_8

1 Mar 2012 to 1 Mar 2012	Palo Alto	United States	South Korea: Navigating the Regulatory and Clinical Trial Environment
This 6-hr virtual seminar will focus on the regulatory compliance requirements and procedures for conducting Clinical Trials on Pharmaceutical Products in South Korea. It will also cover topics relating to pre-clinical and clinical requirements and a...read more Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702153?channel=epmevents

3 Mar 2012 to 4 Mar 2012	Bangalore	India	Future Perspectives in Pharmacovigilance
HIGHLIGHTS Ask the Experts - Join international pharmacovigilance experts for an open Q&A session to discuss your most difficult pharmacovigilance challenges. DIA Special Interest Area Communities (SIACs) FEATURED TOPICS • Safety Management d...read more Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=29003&eventType=Meeting

6 Mar 2012 to 6 Mar 2012	Palo Alto	United States	Software Verification and Validation Planning and Implementation
This Software Verification and Validation training will help you understand and recognize the most common software V&V failings and their fixes. You will learn how to develop and use a repeatable software V&V template for all software validation proj...read more Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701694?channel=epmevents

8 Mar 2012 to 9 Mar 2012	Barcelona	Spain	DIA Training Course on Building the eCTD: Practical Approaches to Compiling Electronic Submissions
During this interactive workshop participants will learn about the Electronic Common Technical Document (eCTD), its components and history, preparing submission ready documents, as well as best practices for changing your business processes in prep...read more Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=28933&eventType=Training Course

11 Mar 2012 to 14 Mar 2012	Irvine	United States	Regulatory Affairs Part I & II: The IND and NDA Phases
Overview: Learn about FDA regulations and expectations for the content, submission, and review of IND/NDAs and the importance of regulatory strategy. What you will Learn Fundamentals of the Investigational New Drug and New Drug Applica...read more Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=28604&eventType=Training Course

12 Mar 2012 to 14 Mar 2012	Horsham	United States	Premarketing Clinical Safety and Pharmacovigilance
Learn how to comply with FDA and European regulations for clinical safety. What you will learn · Fundamental concepts of drug safety and Pharmacovigilance and their application to clinical development · How to comply with F...read more Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=28605&eventType=Training Course

13 Mar 2012 to 14 Mar 2012	Silver Springs	United States	FDA Information Day: Individual Case Safety Reports (ICSR)
The FDA is organizing these two Information Day events to provide the latest information about the Individual Case Safety Reports (ICSR) and the Identification of Medicinal Product (IDMP) Standards. The first part on ICSR will focus on the progres...read more Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=28283&eventType=Meeting

14 Mar 2012 to 15 Mar 2012	Washington, DC	United States	Comparative Effectiveness: A Real-World User's Guide
This meeting will highlight the changing nature of evidence standards within the marketplace; specifi cally, the continued push for increased levels of evidence of comparative eff ectiveness applied within health technology assessments (HTAs). The...read more Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=28862&eventType=Meeting

14 Mar 2012 to 16 Mar 2012	Berlin	Germany	Biostatistics for Non-Statisticians
This three-day session is designed as an introduction to the statistical principles that form the basis for design and analysis of research investigations. The first day will emphasize the principles of descriptive and inferential statistical applica...read more Event Website http://www.cfpie.com/showitem.aspx?productid=010&source=pe

14 Mar 2012 to 16 Mar 2012	Berlin	Germany	The Drug Development Process - from Discovery to Commercialization
This course provides an understanding of the interrelated activities throughout the drug development cycle, and is designed for anyone interested in learning how drugs are developed, manufactured and subsequently brought to market. This course serves...read more Event Website http://www.cfpie.com/showitem.aspx?productid=025&source=pe

14 Mar 2012 to 15 Mar 2012	Silver Springs	United States	FDA Information Day: Identification of Medicinal Products (IDMP)
The FDA is organizing these two Information Day events to provide the latest information about the Individual Case Safety Reports (ICSR) and the Identification of Medicinal Product (IDMP) Standards. The first part on ICSR will focus on the progres...read more Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=28284&eventType=Meeting

14 Mar 2012 to 15 Mar 2012	Horsham	United States	Postmarketing Drug Safety and Pharmacovigilance
An In-depth Look at Practical Solutions to Postmarketing Safety and Pharmacovigilance Learn the key tools available for Pharmacovigilance, discuss their uses, and consider the future directions of the field. What you will learn · Ho...read more Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=28617&eventType=Training%20Course

14 Mar 2012 to 16 Mar 2012	Beijing	China	CTD Dossier - Global Quality, China and EU Module 1 Requirements
The course is designed to introduce requirements, process, and techniques for preparing successful and high quality registration dossiers for regulatory submissions. The Modules provide a comprehensive description on the Common Technical Dossier str...read more Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=29189&eventType=Training%20Course

16 Mar 2012 to 16 Mar 2012	Palo Alto	United States	US, EU and Japan GMP Requirements: Practical ICH Area Differences, Healthcare Authority Inspection Focus
This 6 hour virtual seminar will help you gain a comprehensive understanding of ICH GMPs and the nuances and differences between requirements in the US, EU and Japan. It will prepare you for regulatory inspections in these countries....read more Event Website www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702029?channel=epmevents

16 Mar 2012 to 16 Mar 2012	Palo Alto	United States	Understanding Disinfection and Cleanroom Cleaning in a FDA Regulated Environment
This 90-minute webinar on Disinfection and Cleanroom Cleaning will cover effective ways to rotate disinfectants, most current industry methods for applying disinfectants and effective methods for controlling residues....read more Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701767?channel=epmevents

19 Mar 2012 to 21 Mar 2012	Amsterdam	Netherlands	Freeze Drying Technology
Lyophilisation, or freeze drying, is an important process in many areas of research and production with applications in areas such as vaccines, diagnostics, regenerative medicine, functional foods, materials science and medical devices. BTL’s train...read more Event Website http://www.biopharma.co.uk/training-courses

19 Mar 2012 to 21 Mar 2012	Dublin	Ireland	cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
This three-day course is designed for anyone who works in a current Good Manufacturing Practices (cGMP) environment, and anyone who needs to understand the concepts of cGMP and quality in a manufacturing setting. Participants will gain a thorough un...read more Event Website http://www.cfpie.com/showitem.aspx?productid=095&source=pe

19 Mar 2012 to 21 Mar 2012	Dublin	Ireland	Lyophilization Technology - Practical Application of the Scientific Principles
This three-day course is designed for those in the pharmaceutical, biomedical, medical device/diagnostic, and biotechnology industries who develop and/or produce lyophilized (freeze-dried) products. Upon completion of this course, attendees will have...read more Event Website http://www.cfpie.com/showitem.aspx?productid=128&source=pe

19 Mar 2012 to 21 Mar 2012	Berlin	Germany	Good Clinical Practices (GCPs)
This course is designed for Clinical Research Monitors (CRMs), Clinical Research Auditors and others who need basic and expanded knowledge in FDA and ICH regulations for Good Clinical Practices (GCPs). This three-day program will provide attendees wi...read more Event Website http://www.cfpie.com/showitem.aspx?productid=039&source=pe

19 Mar 2012 to 20 Mar 2012	Horsham	United States	Regulatory Affairs for Biologics
Discuss proven strategies to achieve regulatory compliance for the development of biologics. What you will learn Difference between traditional biologics and biotechnology products Regulatory needs and requirements for biologics Unique...read more Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=28619&eventType=Training%20Course

20 Mar 2012 to 22 Mar 2012	Moscow	Russia	Cool Chain Logistics Russia and CIS
Following on from our flagship Cool Chain conferences that are run in over 10 locations globally and attended by 100s of leading industry players, Pharma IQ is proud to brings you the very latest in the series, Cool Chain Logistics Russia and CIS. Wi...read more Event Website www.coolchainrussia.com

20 Mar 2012 to 22 Mar 2012	Cologne	Germany	Green Polymer Chemistry 2012
AMI's 1st international conference on Green Chemistry in the polymer industry will take place from 20-22 March 2012 at the Maritim Hotel in Cologne, Germany. Green Polymer Chemistry 2012 provides a forum for environment and sustainability managers, b...read more Event Website http://www2.amiplastics.com/Events/Event.aspx?code=C412&sec=1853

21 Mar 2012 to 23 Mar 2012	Tokyo	Japan	CPhI Japan
CPhI for Pharmaceutical Ingredients...read more Event Website www.cphijapan.com

21 Mar 2012 to 23 Mar 2012	Tokyo	Japan	ICSE Japan
ICSE for International Contract Services...read more Event Website www.icsejapan.com

21 Mar 2012 to 23 Mar 2012	Tokyo	Japan	P-MEC Japan
P-MEC for Pharmaceutical Machinery, Equipment and Technology...read more Event Website www.pmec-japan.com

21 Mar 2012 to 23 Mar 2012	Tokyo	Japan	BioPh Japan
BioPh for Bio-solutions for Pharma....read more Event Website www.biophjapan.com

25 Mar 2012 to 25 Mar 2012	Copenhagen	Denmark	Training course on Quality Risk Management (QRM)
This course will deliver an in-depth overview to risk based quality management on how to assess risk and improve quality in your organisation. As an introduction, general risk management concepts and methodologies will be presented as the basis for Q...read more Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=28403&eventType=Training Course

26 Mar 2012 to 27 Mar 2012	Dublin	Ireland	Process Validation for Drugs and Biologics
Participation will be beneficial to personnel directly involved in process/product development, manufacturing, quality control/assurance and process validation. By the end of this course, attendees will be able to understand the new FDA perspective ...read more Event Website http://www.cfpie.com/showitem.aspx?productid=049&source=pe

27 Mar 2012 to 29 Mar 2012	Beckenham, Kent, Nr London	United Kingdom	Hands-on Tablet Development including principles of pre-formulation, formulation and process development (3 day)
This unique 3 day course is designed to integrate the key elements of tablet development with hands-on, practical experience in a small scale, lab scale test facility. Each day will consist of lectures on aspects of tablet development, followed by li...read more Event Website http://www.pharma-training-courses.com/hands-on-tablet-development-including-the-principles-of-pre-formulation-formulation-and-process-dev_28.htm

28 Mar 2012 to 29 Mar 2012	Dublin	Ireland	Comprehensive Overview of FDA Regulatory Compliance for Medical Devices
This two-day course has been developed for those who are involved with ensuring regulatory compliance for medical devices. The course is primarily geared towards those who are new to industry or require a basic understanding of medical device regula...read more Event Website http://www.cfpie.com/showitem.aspx?productid=020&source=pe

29 Mar 2012 to 30 Mar 2012	Dublin	Ireland	EU Filing and Registration Procedures
This course will give participants the necessary overview of the applications and procedures used within Europe to grant marketing authorizations for medicinal products, as well as, the agencies and institutions which control the regulatory process. ...read more Event Website http://www.cfpie.com/showitem.aspx?productid=031&source=pe

30 Mar 2012 to 30 Mar 2012	Palo Alto	United States	Quality Agreements with Pharmaceutical/ Biologic Manufacturers and the Use of Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilities
This combined Quality Agreement and DMF (Drug Master Files) training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together....read more Event Website www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702171?channel=epmevents

4 Apr 2012 to 4 Apr 2012	Palo Alto	United States	Validation and Use of Excel® Spreadsheets in Regulated Environments
This excel validation training/ webinar will demonstrate how to design spreadsheets for part 11/GxP /SOX/HIPAA, document planning, specifications, installation, testing and changes to meet FDA requirements....read more Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701242?channel=epmevents

6 Apr 2012 to 6 Apr 2012	Palo Alto	United States	Understanding Disinfectant Qualification Studies – How to Avoid Errors
This 90-minute webinar on Disinfectant Qualification Studies will teach you disinfectant testing methodologies, provide examples of disinfectant efficacy tests and show how to troubleshoot problems related to disinfectant efficacy testing....read more Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702210?channel=epmevents

12 Apr 2012 to 13 Apr 2012	Berlin	Germany	Development and Validation of Bioanalytical Assays for Biologics: Quantification (PK) and Immunogenicity Assays
This two-day course is designed for those who perform, supervise, manage, audit, or oversee the validation of bioanalytical assays in a GLP laboratory. Upon completion of this course, participants will have a detailed understanding of regulatory agen...read more Event Website http://www.cfpie.com/showitem.aspx?productid=114&source=pe

13 Apr 2012 to 14 Apr 2012	Mumbai	India	5th Regulatory Conference: Evolving Global Regulatory Requirements Environment
Pharmaceutical manufacturers in India are facing many challenges within the domestic and global regulatory environment. These challenges include manufacturing and quality control, testing and packaging. This conference will provide interactive sessio...read more Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=29004&eventType=Meeting

17 Apr 2012 to 18 Apr 2012	Washington, DC	United States	Cardiovascular Safety and State-of-the-art Development Issues: Type 2 Diabetes Mellitus Medications, QT, Benefit/Risk Assessment, Arrhythmias, Thrombosis, and Cardiotoxicity
Type 2 Diabetes Mellitus Medications, QT, Benefit/Risk Assessment, Arrhythmias, Thrombosis, and Cardiotoxicity Join Industry Experts and Regulators to Improve Your Safety Analysis During Drug Development, Analyze and Mitigate Potential Risks, and ...read more Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=28857&eventType=Meeting

19 Apr 2012 to 20 Apr 2012	Berlin	Germany	Effective Document Management for the Pharmaceutical, Biotech and Medical Device Industries
This course will be of benefit to pharma, medical device, and biotech professionals who manage documents for all therapeutic product development and marketing activities (including pre-clinical, clinical, QA, and regulatory functions). This two-day c...read more Event Website http://www.cfpie.com/showitem.aspx?productid=027&source=pe

23 Apr 2012 to 25 Apr 2012	Berlin	Germany	Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
Scientists, engineers, and technicians in research and development will find this course valuable, as will quality assurance (QA), information technology (IT), manufacturing, and other operations professionals. Course notes and interactive exercise...read more Event Website http://www.cfpie.com/showitem.aspx?productid=077&source=pe

23 Apr 2012 to 24 Apr 2012	Berlin	Germany	Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
This two-day course provides comprehensive and up-to-date knowledge of assay validation for quality assurance and control of pharmaceuticals, biopharmaceuticals, and biologics. The course covers regulatory expectations regarding validation as contain...read more Event Website http://www.cfpie.com/showitem.aspx?productid=096&source=pe

24 Apr 2012 to 26 Apr 2012	Geneva	Switzerland	LogiPharma 2012
LogiPharma Europe 2012 24th – 26th April 2012 – 2 day main conference + Focus Day Geneva The 11th annual LogiPharma Europe 2012 is the only end-to-end pharma supply chain conference where strategic-level BioPharma logistics professionals meet...read more Event Website www.logipharmaeurope.com

24 Apr 2012 to 25 Apr 2012	Philadelphia	United States	Clinical Data Quality Summit
This meeting will include a mix of plenary and breakout sessions designed to be highly interactive working sessions. You will: • Troubleshoot, share processes and exchange ideas with colleagues from various clinical areas • Explore new tools, techn...read more Event Website http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?productID=28850&eventType=Meeting

24 Apr 2012 to 24 Apr 2012	Palo Alto	United States	Excel Spreadsheets; develop and validate for 21 CFR Part 11 compliance
How to Use excel spreadsheet for GXP data and reduce validation cost and time. Why Should You Attend: Learn how to create an Excel spreadsheet application that is GxP compliant. Understand how to validate your application with minimal documentati...read more Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701582?channel=epmevents

25 Apr 2012 to 27 Apr 2012	Berlin	Germany	QA/QC Strategy for Biopharmaceuticals and Biologics
The course is designed for management and professional staff involved in – or interested in – quality assurance (QA) and quality control (QC) support for biologics and biopharmaceuticals. Curriculum highlights the challenges and pressures facing QA/...read more Event Website http://www.cfpie.com/showitem.aspx?productid=065&source=pe

25 Apr 2012	Daventry	UK	Synergy Health Electron Beam Education Day
Electron beams are used to meet many different market requirements such as, sterilization, contamination control, enhancing product characteristics and polymer modification. Compared to other forms of irradiation, Electron ...read more Event Website www.synergyhealthplc.com/sterilisation

26 Apr 2012 to 27 Apr 2012	Berlin	Germany	Writing Effective Standard Operating Procedures and Other Process Documents
This is a course for people who must write process documents required by FDA and international regulations. Process documents create a procedural infrastructure that delineates the company’s activities. These documents include Standard Operating Proc...read more Event Website http://www.cfpie.com/showitem.aspx?productid=083&source=pe

26 Apr 2012 to 28 Apr 2012	Greater Noida	India	India Cold Storage Show 2012
India Cold Storage Show 2012 at India Expo Centre, Greater Noida to be held from 26-28 April 2012-an exciting event to look out for, with major players participating in the Show to promote new technologically improved temperature controlled Storages ...read more Event Website http://www.indiacoldstorageshow.com/

3 May 2012 to 4 May 2012	Berlin	Germany	Pharma Outsourcing & Procurement Summit 2012
Pharmaceutical outsourcing is growing exponentially amidst challenging price restrictions, US health care reforms and reduced revenues. The pharmaceutical and outsourcing summit addresses the urgent need for pharma to identify and locate the best ou...read more Event Website www.outsourcingevent.com

7 May 2012 to 8 May 2012	Berlin	Germany	Validation of Computer Systems
This course is designed for Validation, Quality, IT, and business personnel responsible for implementing and using regulated computer systems in the pharmaceutical, biotech and medical device industries. Participants will gain a thorough understandin...read more Event Website http://www.cfpie.com/showitem.aspx?productid=081&source=pe

14 May 2012 to 15 May 2012	Dublin	Ireland	Medical Devices – EU Directives Guidance CE Marking and ISO Standard Certifications
The European Union (EU) provides an attractive marketplace for medical device distribution. Development of requirements harmonized across the 27 member states should make it a straightforward process to get products approved in each country - but is ...read more Event Website http://www.cfpie.com/showitem.aspx?productid=094&source=pe

16 May 2012 to 17 May 2012	Dublin	Ireland	Practical Methods for Project Management
This workshop will be of great value to those in the life sciences, consumer products, food, and chemical industries who are responsible for directing projects within their areas of expertise. This is especially valuable for technical personnel with ...read more Event Website http://www.cfpie.com/showitem.aspx?productid=060&source=pe

16 May 2012	London	United Kingdom	How to Audit API Manufacturers (1 day)
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/EC. QPs are required to declare that the active materials used in each of their products...read more Event Website http://www.pharma-training-courses.com/how-to-audit-api-manufacturers_18.htm

17 May 2012 to 18 May 2012	Dublin	Ireland	Medical Devices – Developing Effective Post Market Surveillance and Complaint Handling Systems
This course will be of great value to medical device professionals involved in post market surveillance. Upon completion of this course, participants will understand all the processes involved in post market surveillance, as well as the requirements ...read more Event Website http://www.cfpie.com/showitem.aspx?productid=092&source=pe

21 May 2012 to 22 May 2012	Dublin	Ireland	FDA Inspections -What Regulators Expect and How to Prepare
This two-day course is a practical, hands-on program designed to provide pharmaceutical, biopharmaceutical, biologics, and medical device professionals with the information and tools they require to prepare for and manage an FDA inspection. The cour...read more Event Website http://www.cfpie.com/showitem.aspx?productid=033&source=pe

21 May 2012 to 22 May 2012	Dublin	Ireland	Medical Devices – Field Actions and Their Management - Recalls, Product Recovery, Safety Alert
Field actions are a difficult yet necessary aspect of the medical device marketplace. The various stakeholders: regulatory agencies, physicians, users, patients, organizations and personnel are all affected but in different ways, having different re...read more Event Website http://www.cfpie.com/showitem.aspx?productid=091&source=pe

11 Jun 2012 to 12 Jun 2012	Laupheim	Germany	2. Laupheimer Zelltage
Second Industrial Cell Culture Technology Conference The biennial Laupheimer Zelltage provide comprehensive scientific updates on cutting-edge technologies for industrial cell culture technology professionals. Academic and industrial experts in...read more Event Website www.laupheimer-zelltage.org

19 Jun 2012 to 19 Jun 2012	Palo Alto	United States	Reduce COTS Software Validation using the risk-based approach
Understand 10 step Risk based approach to validation, explore methods to decrease resource requirements and make documentation more manageable and understandable....read more Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701583?channel=epmevents

24 Jun 2012 to 28 Jun 2012	Philadelphia	United States	DIA 2012: Collaborate to Innovate
DIA 2012: Collaborate to Innovate is the largest multidisciplinary event that brings together a global network of professionals to foster innovation that will lead to the development of safe and effective health care products. Through increased ac...read more Event Website http://www.diahome.org/DIAHOME/FlagshipMeetings/PostSesProf.aspx?meetingid=27170

26 Jun 2012 to 28 Jun 2012	Shanghai	China	CPhI, ICSE, P-MEC, InnoPack China
CPhI for Pharmaceutical Ingredients, ICSE for International Pharmaceutical Contract Services, P-MEC for Pharmaceutical Machinery, Equipment and Technology and InnoPack for Innovative Pharmaceutical Packaging Solutions....read more Event Website www.cphi-china.com/icb

18 Sep 2012 to 18 Sep 2012	Palo Alto	United States	Risk Assessment-Compliance Using Easy To Fill Out Documentation
Learn how to perform risk assessment as part of the risk-based approach to computer system validation. Why Should You Attend: This webinar will show how you can determine and document risk in a process to reduce system validation time and ensur...read more Event Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=700896?channel=epmevents

25 Sep 2012 to 26 Sep 2012	Birmingham	UK	MM, MEMS & NANO Live 2012
Reflecting on the growing trend toward product miniaturisation across an increasing number of manufacturing sectors, MM LIVE, MEMS LIVE and NANO LIVE have rapidly grown to become one of Europe’s largest annual exhibitions and conferences to focu...read more Event Website www.mmliveuk.com

25 Sep 2012 to 26 Sep 2012	Birmingham	UK	TCT Live 2012 — The International Forum for Product Development and Manufacturing
TCT Live is the event for Product Development and Additive Manufacturing in Europe. The show provides the ideal forum for everyone involved in the concept, design, specification and manufacturing process to learn about the latest in Additive Man...read more Event Website www.tctshow.com

25 Sep 2012 to 26 Sep 2012	Birmingham	UK	Mediplas 2012 — Specifically Medical, Specifically Plastics
Mediplas is a NEW uniquely focused event for the highly specialised area of manufacturing plastic parts for the medical industry. The exhibition will cover all areas of the medical plastics supply chain. Plastics production for the medical indus...read more Event Website www.mediplasuk.com

12 Oct 2012 to 14 Oct 2012	Dubai	UAE	Dubai International Pharmaceuticals & Technologies Confernece & Exhibition - DUPHAT 2012
The 17th Dubai International Pharmaceutical & Technologies Conference & Exhibition -DUPHAT 2012 will be held from 12 - 14 March 2012. DUPHAT is the largest pharma industry specialized event in the Middle East. ...read more Event Website www.duphat.ae

30 Sep 2014 to 2 Dec 2014	Birmingham	UK	INTERPLAS 2014 — The International Forum for the British Plastics Industry
Interplas was organised by Rapid News communications Group for the first time in 2011 and is The leading triennial plastics exhibition and has successfully represented the UK plastics industry for over 60 years. The exhibition will cover a...read more Event Website www.britishplasticsshow.com