This 2-hr webinar will provide a comprehensive overview of impurities in pharmaceutical products, that require to be controlled, and the strategies for controlling them.
Why Should You Attend:
This webinar is designed to provide an overview of impurities which must be controlled in pharmaceutical products, detailed review of the guidance documents related to each of the categories of impurities and strategies to address each, including reporting of test results. We will discuss drug-related impurities, including process impurities, normal degradation products and potential genotoxic impurities and general impurities (not structurally related to the drug substance), such as residual solvents and elemental impurities.
Date: August 22, 2012
Time: 10:00 AM -12:00 PM PDT
Cost: $299 per attendee per computer terminal
Registration: SIgn-Up on-line now. Add to your shopping cart.
Added by complianceonlinecom on August 8, 2012