FDAnews Post-Marketing Surveillance Conference
Date & Time
June 28, 2019 8:00 AM - 4:00 PM
- Event Type
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Structured as a workshop for drug, biologics, device, and diagnostics makers, the conference will explore the programs FDA uses to regulate medical products after launch in order to monitor for unexpected adverse events and potential threats to public health. Brian will participate in a panel about drug pharmacovigilance under FDA’s Center for Drug Evaluation and Research alongside Cynthia Schnedar, Greenleaf Health’s Executive Vice President of Regulatory Compliance. Drawing on over 20 years of food and drug law experience, Brian will offer guidance about complying with agency rules and avoiding product liability litigation. Paula Katz, Special Counsel at Covington & Burling will be moderating the panel.
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