Medical Devices: Section 522 of the FD&C Act Course: Developing Effective Post Market Surveillance and Complaint Handling Systems Training (Jan 22nd - Jan 23rd, 2026 & On-Demand)

The market opportunity lies in providing solutions and services for global medical device companies to comply with US FDA and EU MDR post-market surveillance and complaint handling requirements. This ...
Business Wire

Virtual Course: Developing Effective Medical Devices Post Market Surveillance and Complaint Handling Systems Under Section 522 of the Federal Food, Drug, and Cosmetic Act (FD&C ...

DUBLIN--(BUSINESS WIRE)--The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems" training has been added to ...
Business Wire

Medical Devices Post Market Surveillance and Complaint Handling Systems Course: U.S. FDA CGMP Expectations/Requirements (ONLINE EVENT/ON-DEMAND) - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Course" training has been added to ResearchAndMarkets.com's offering. This ...
KOIN 6

FDA took months to react to complaint about Abbott infant formula factory, audit finds

This is an archived article and the information in the article may be outdated. Please look at the time stamp on the story to see when it was last updated. The U.S. Food and Drug Administration took ...