July 15, 2020
Dr. Weiss is an epidemiologist with 25 years of experience in pharmacoepidemiology and regulatory sciences. She specializes in the safety of FDA-regulated medical products, drugs, biologics, vaccines, devices, and combination products. Dr. Weiss works with pharmaceutical companies to develop, articulate, and optimize safety strategies at all phases of a product lifecycle, from pre-approval through post-marketing. In addition to conducting epidemiological studies, she works on the design and evaluation of registries, risk evaluation and mitigation strategies (REMS), and pharmacovigilance signal detection strategies/enhanced pharmacovigilance of adverse events. Dr. Weiss serves as a consultant and expert witness on litigation involving the safety of regulated medical products.