In June 2025, the US Food and Drug Administration (FDA) announced a major update to its General Food Labeling Requirements Compliance Program—the first overhaul of this program since 2010. This ...

In this podcast, Jason Reddish, Principal and Mark Ogunsusi, Associate, at Powers Pyles Sutter & Verville provide an overview of the program and the compliance requirements. They are also two of the ...

The CNPV program aims to reduce drug review times to 1-2 months, raising concerns about safety and regulatory scrutiny. Critics argue that accelerated timelines may lead to safety issues and strain ...

The Food and Drug Administration (FDA) lacks certain authorities and is persistently underresourced to fulfill its mission of protecting the public by ensuring that foods are safe, wholesome, sanitary ...

The "FDA Regulatory Compliance for Drug and Biotech Products (Nov 12th - Nov 13th, 2025)" training has been added to ResearchAndMarkets.com's offering. Regulatory Compliance is the level of activity ...

First step in Transforming Product Quality for a Safer World At Innova-Q our goal is to transform product quality for a safer world. The launch of the In-Q Center is the first of many innovations that ...

A gene therapy for hearing loss. A drug that helps people quit e-cigarettes or vaping. An anesthetic whose main ingredient will be manufactured in the U.S. These are among the first nine therapies ...

ORLANDO, Fla. — The FDA is initiating a program to improve retailer compliance in order to fight youth vaping, focusing on vape shops, convenience stores, and gas stations nationwide. The initiative ...

FDA is a regulatory agency, and it must be able to validate the company’s compliance with any regulatory program. So given that the focus of the excellence appraisal is much broader and covers a range ...

The FDA’s Center for Devices and Radiological Health plans to expand its digital health pre-certification pilot program by the end of 2018, the center’s associate director for digital health Bakul ...