Pharmaceuticals 2011 - Addressing Impurities in Pharmaceutical Products - Webinar by ComplianceOnline
Date2011-10-20
Deadline2011-10-20
VenuePalo Alto, USA - United States
KeywordsPharmaceutical Products;General Impurities; Residual Solvents;PPM; PDE Drug Related Impurities;Process Impurities
Topics/Call fo Papers
This 7-hr webinar on Impurities in Pharmaceutical Products will provide a comprehensive overview of impurities which must be controlled in pharmaceutical products and the strategies for controlling them.
Why Should You Attend:
This webinar is designed to provide a comprehensive 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. Topics for discussion include general impurities (not structurally related to the drug substance), such as residual solvents, elemental impurities, and microbial issues, and drug-related impurities, including process impurities, normal degradation products and potential genotoxic impurities.
Interaction and questions from the participants are actively encouraged throughout, and there will be ample time for questions at the end of the presentation.
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Last modified: 2011-09-29 16:38:11