Drug Information Association/FDA Co-Sponsored Conference Discusses Use (Q)Sar to Assess Impurities for Potential Genotoxicity
- Strategies for Classifying and Controlling Potentially Genotoxic Impurities in the Pharmaceutical Industry
- Regulatory Perspectives: FDA, EU, and Japan
- What Current (Q)SAR Computational Models Can Tell Us about Ames Predictivity
- Industry Use of (Q)SAR: Overview and Case Studies
- Integration of (Q)SAR into Hazard Identification: Role of ICH
Dr. David Jacobson-Kram, Associate Director of Pharmacology and Toxicology, Office of New Drugs (OND), CDER, FDA, will deliver the keynote address titled: “Use of in Silico Analyses for Mutagenicity Predictions: State-of-the-Art and Regulatory Implications.”
Since 1976, Dr. Jacobson-Kram has published more than 80 abstracts, 60 peer-reviewed articles, and 30 review articles or book chapters. The majority of these publications deal which methods and issues in genetic and molecular toxicology. Register for DIA/FDA Quantitative Structure-activity Relationship (Q)SAR Approaches to Assessing Genotoxic Impurities in Pharmaceuticals.
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