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July 30, 2026
How a strong postmarketing surveillance partnership protects your consumers, your program, and your business The terms you'll see in this article ICSR (Individual Case Safety Report) — the formal record…
April 16, 2026
April 16, 2026 | FDA Adverse Event Reporting Services: A Step-by-Step Process Guide When a reportable adverse event reaches your organization, the first question is: how much time do you…
April 16, 2026
April 29, 2026 | Cosmetic Adverse Event Reporting Under MoCRA TLDR: Key Takeaways The Modernization of Cosmetics Regulation Act (MoCRA) requires the designated “Responsible Person” for a cosmetic product to…
April 16, 2026
May 8, 2026 | Dietary Supplement Adverse Event Reporting Under DSHEA TLDR: Key Takeaways The Dietary Supplement and Nonprescription Drug Consumer Protection Act requires manufacturers, packers, and distributors whose name…
April 15, 2026
April 16, 2026 | Adverse Event Management Services: Comprehensive FDA Solutions for Regulatory Compliance TL;DR, Key Takeaways Adverse event (AE) management is a regulatory requirement... Reporting timelines vary by product…
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