WCDG & AOAC-SCS Joint Two-Day Regulatory & Compliance Conference , Nov. 5–6, 2009

 Strategies and Challenges for Raw Materials Qualification in Pharmaceutical Product Development

 Overview of the Pharmacopeial Discussion Group: Harmonization from a Compendial Perspective 

 Good Storage and Shipping Practices for Drug Products

 Aggregates in Therapeutic Protein Products 

 Extractable/Leachable Testing & Regulatory Requirements for Ophthalmic Dosage Forms

 USP's Elemental Impurities Initiative - Current Status 

 Heavy Metals Update

 Impurity Profiling 

 The Evaluation of Impurities in Investigational New Drug and New Drug Applications

 What Does Quality By Design Bring to your Drug Development Program? 

 Biological Raw Material Contaminants

AOAC / WCDG meeting , May 7–8, 2009

 Understanding DS cGMP Requirements for Testing

 Assuring the Quality of Dietary Supplements and Functional Ingredients 

 Microbiology Challenges Under New Dietary Supplement GMPs 

 Qualify 3rd Party Lab and Understand Conflicting Lab Results 

 Detection of Pharmaceutical Drugs & Related Analogues in Dietary Supplements 

 Canadian Regulatory Requirements for Natural Health Products: An Industry Perspective 

 Approaches to Regulating Dietary Supplements and their Claims 

  Ensuring a Method is Ensuring a Method is "Fit for Purpose Fit for Purpose" 

Inaugural Research Symposium, April 20-21, 2009

USP WCDG Meeting Agenda, March 6, 2009

2008 and older USP updates and events...