MD&M East

FDA’s Registration List is Changing. Should You Be on It?

FDASIA was signed into law on July 9, 2012. This piece of legislation grants FDA the authority to collect user fees from industry to fund reviews of drugs, devices, and biologics. The changes to ...
Politifact

A product says it's ‘FDA approved,’ ‘FDA registered’ or ‘FDA certified.’ What does that even mean?

An Instagram ad catches your eye. You click to the product’s website and find reassurance: The product, it says, is "FDA certified" or was "produced in an FDA registered facility." Mention of the U.S.
JD Supra

MOCRA: FDA Draft Guidance on Facility Registration and Product Listing

As we previously discussed, MoCRA requires cosmetic product manufacturer and processors to register their facilities with the U.S. Food and Drug Administration (FDA). On August 7, 2023, FDA announced ...
JD Supra

Cosmetics Update: FDA Publishes Draft Guidance on Cosmetic Product Facility Registration and Listing

Our FDA and Food & Beverage teams outline key requirements of the Modernization of Cosmetics Regulation Act (MoCRA) and provide key takeaways from the Food and Drug Administration’s new draft guidance ...
Pharmaceutical Technology on MSN

Navigating the FDA’s import operations for pharmaceuticals and biologics

An FDA officer explains the agency’s compliance requirements for importing pharmaceuticals and biologics and processes.
The National Law Review

FDA Amends Final Rule on Registration of Food Facilities

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 ...
The National Law Review

FDA Webinar on Food Facility Registration

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 ...