On-Demand Catalog

All sessions average between 60 and 90 minutes.

USDA’s Proposed Bioengineered Food Disclosure Standard
DEA Law for the Food and Drug Community
Data Integrity: FDA Enforcement and Risk-Reduction Considerations
First Amendment Issues in Advertising and Product Packaging Webinar
New Medical Device Requirements and Where Manufacturers Should Focus: MDUFA, FDARA, and 21st Century Cures
Real World Evidence: Data Requirements, Utilization, and Presentation
Editorial or Ad? FTC’s Native Advertising Guidelines and Challenges for Industry
Development of Medical Devices: Best Practices for Safeguarding Your IP and FDA Rights
FDA, USDA, and EPA: Inter-Agency Overlap and Jurisdictional Boundaries
PDUFA and BsUFA Reauthorization: Key Changes Affecting Industry and Patients

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