Thursday February 23, 2012
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Date Time Event
Feb 22, 2012 1:00 PM ET Development, Validation, Verification and Transfer of Analytical Methods (Series 1)
Feb 23, 2012 1:00 PM ET Development, Validation, Verification and Transfer of Analytical Methods (Series 2)
Feb 24, 2012 10:00 AM ET Analytical Standards: The Ultimate Control
Feb 24, 2012 1:00 PM ET The FDA Pharmaceutical (Drug & Biologics) GMP
Feb 28, 2012 10:00 AM ET Implementing Changes: Monitoring for Success Top 15 Factors to Consider When Implementing Changes in your Organizations
Feb 28, 2012 1:00 PM ET Successful Computer Validation Module 2
Mar 1, 2012 1:00 PM ET Developing an Environmental Plan for a Controlled/Classified Environment
Mar 2, 2012 1:00 PM ET Cleaning for Dietary Supplements/Nutraceuticals Facilities
Mar 7, 2012 1:00 PM ET Basics of Cold-Chain Distribution Management - Module 1
Mar 8, 2012 1:00 PM ET European Regulatory Affairs Series 3: Examine the Centralized Procedure
Mar 13, 2012 1:00 PM ET Dietary Supplement Basics: Selling Supplements in the United States
Mar 14, 2012 1:00 PM ET An Overview of Aseptic Processing
Mar 16, 2012 1:00 PM ET Training that Counts – How to Design Learning Plans
Mar 19, 2012 10:00 AM ET FDA Expectations for Microbial Control of Biopharmaceutical Processes
Mar 20, 2012 1:00 PM ET Successful Computer Validation Module 3
Mar 22, 2012 1:00 PM ET Equipment Qualification as a Foundation for Process Validation
Mar 23, 2012 10:00 AM ET Records and Information Management Fundamentals Module 1
Mar 23, 2012 1:00 PM ET Designing Clinical Trials for Pharmaceuticals
Mar 27, 2012 10:00 AM ET Natural Health Products Basics: Selling Supplements in Canada
Mar 28, 2012 1:00 PM ET Forms for the Pharmaceutical, Biologics, Medical Device and Diagnostic Fields - Considerations to Make Forms More User Friendly While Reducing Error Entries
Mar 29, 2012 1:00 PM ET FDA Process Validation Guidance – The New Gold Standard
Mar 29, 2012 1:00 PM ET Basics of Cold-Chain Distribution Management - Module 2
Mar 30, 2012 10:00 AM ET Phase-focused CMC Strategy for Small Pharma
Mar 30, 2012 1:00 PM ET The Mind at Work – How it Works and Why Mistakes Happen
Apr 2, 2012 1:00 PM ET For the CMC Scientist: FDA-Sponsor Meetings
Apr 3, 2012 1:00 PM ET European Regulatory Affairs Series 4: Introduction to EU Medical devices Regulations
Apr 13, 2012 10:00 AM ET Records and Information Management - Intellectual Property Module 2
Apr 13, 2012 1:00 PM ET FDA’s Bioresearch Monitoring Program (BIMO): FDA Inspections for GCP, GLP, GMP
Apr 17, 2012 1:00 PM ET Successful Computer Validation Module 4
Apr 25, 2012 1:00 PM ET European Regulatory Affairs Series 5: Medical device clinical evaluations and investigations
Apr 27, 2012 10:00 AM ET Records and Information Management Fundamentals for Regulatory Compliance Module 3
May 11, 2012 10:00 AM ET Long Term Preservation Strategies for Essential Records Module 4
May 11, 2012 1:00 PM ET European Regulatory Affairs Series 6: Vigilance and PMS
May 25, 2012 1:00 PM ET Designing Clinical Trials for Medical Devices
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