Using Individual Case Safety Reports in FAERS for Regulatory Decision Making
- Non-Members - Free!
- Members - Free!
Speaker: Monica Munoz, PharmD, PhD
Adverse event reporting systems like the FDA Adverse Event Reporting System (FAERS) are designed to support postmarketing safety surveillance programs for drug and biological products. This webinar will provide an overview and examples of how individual case safety reports in FAERS inform regulatory decision-making.