Yahoo Finance

US FDA QMSR ( Quality Management System Regulation) Transition Course: Harmonization of 21 CFR 820, Device CGMPs (QSR), to the ISO 13485 (ON-DEMAND)

Dublin, June 28, 2024 (GLOBE NEWSWIRE) -- The "The US FDA QMSR Transition - 21 CFR 820 and ISO 13485" training has been added to ResearchAndMarkets.com's offering. The US FDA, after years of ...
Yahoo Finance

2 Day Training Course | FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Medical Device Manufacturers (ONLINE EVENT: September 22-23, 2025)

Dublin, July 10, 2025 (GLOBE NEWSWIRE) -- The "The FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Medical Device Manufacturers" training has been added to ...
MD&M East

How Will FDA’s New QMSR Affect Medical Device Companies?

On Feb. 2, 2024, FDA published its long-awaited amendment to its current good manufacturing practice requirements for medical devices. The new Quality Management System Regulation (QMSR) now ...
Plastics Today

Medical molder boosts quality program with FDA 21 CFR 820

The company was certified in 2009 to the stringent ISO 13485 standard that requires demonstrating a comprehensive management system for the design and manufacture of medical devices. The FDA 21 CFR ...
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 ...