Business Wire

Cybersecurity and US FDA Requirements Webinar: How Cybersecurity is Introduced into the CGMPs, Design Control (21 CFR 820.30) for Devices, and Post-production by the CAPA ...

DUBLIN--(BUSINESS WIRE)--The "Cybersecurity and US FDA Requirements - Webinar" webinar has been added to ResearchAndMarkets.com's offering. There are regulations such as 21 CFR Part 11 in the U.S. and ...
MD&M East

Packaging Should Be Part of the Design Control Process

It’s important to consider packaging design early on during the medical device product design process, according to Jenn Goff, director of product marketing of Oliver Healthcare Packaging. During the ...