JD Supra

CARES Act Reforms to Address Drug and Device Shortages and Updates to the OTC Drug Monographs

The CARES Act amends section 506C of the Federal Food, Drug, and Cosmetic Act (FDCA) to require manufacturers of either (1) any “drug that is critical to the public health during a public health ...
Yahoo Finance

FDA Regulation for Over-the-Counter (OTC) Drug Products Webinar: Explore Key Aspects Such As Regulatory Frameworks, Approval Processes, Labeling Requirements, and Compliance ...

Dublin, Nov. 05, 2025 (GLOBE NEWSWIRE) -- The "FDA Regulation for Over-the-Counter (OTC) Drug Products (Aug 22, 2025)" training has been added to ResearchAndMarkets.com's offering. This 90-minute ...
The National Law Review

FDA Begins Modernizing its Resources and Implementing Over-The-Counter Monograph User Fee Requirements

We collaborate with the world's leading lawyers to deliver news tailored for you. Sign Up for any (or all) of our 25+ Newsletters. Some states have laws and ethical rules regarding solicitation and ...
PharmTech

Multi-Compendial Compliance for Pharmaceutical Excipients–Part 1: A Practical Application of Specification Equivalence

In-house harmonization of excipient specifications ensures compliance with multiple pharmacopoeias, reducing redundant testing and aligning with global regulatory expectations. Specification ...
Mena FN

FDA Regulation For Over-The-Counter (OTC) Drug Products Webinar: Explore Key Aspects Such As Regulatory Frameworks, Approval Processes, Labeling Requirements, And Compliance ...

(MENAFN- GlobeNewsWire - Nasdaq) The webinar highlights market opportunities in the regulatory landscape for OTC drugs, providing professionals with key insights into FDA requirements, labeling, and ...