JD Supra3h
MoCRA Guidance Update for Registration and Listing of Cosmetic Product Facilities and Products
What Happened: The Food and Drug Administration (FDA) released new guidance regarding the registration and listing of ...
TMCnet1d
Cryoport's MVE Biological Solutions Registers All Manufacturing Facilities with the U.S. Food and Drug Administration ("FDA")
To meet the standards of FDA-registered facilities, MVE adheres to stringent requirements, including but not limited to 21 ...
JD Supra12d
FDA Seeks Comments on Updates to MoCRA Guidance on Registration, Listing of Cosmetic Product Facilities
On December 11, 2024, the US Food and Drug Administration (FDA) updated its Guidance for Industry: Registration and Listing of Cosmetic ...
Contract Pharma23h
Cryoport’s MVE Biological Solutions Registers Mfg. Facilities with FDA
Adheres to requirements, including 21 CFR Part 820 and Good Manufacturing Practices.
FDA 510(K) Approved Facilities: Increasing GMP Inspections And Compliance Requirements
Indian medical device manufacturers are enhancing GMP compliance and embracing proactive strategies to meet rising USFDA ...
Associated Press4mon
Nearly 2,000 drug plants are overdue for FDA checks after COVID delays, AP finds
“We have to recognize that this is the world we live in and we have to adapt to it,” said Dr. Stephen Ostroff, FDA’s former chief scientist. “That has to include being able to get into these ...