MD&M East

Understanding the New EMC Standard for Medical Devices: What Manufacturers Need to Know Now

A test technician prepares for an EMC test in a 10-m semianechoic chamber. Use of a semianechoic chamber is necessary for the immunity testing required under EN 60601-1-2:2001 for applicable medical ...
News-Medical.Net

Medical devices and EU laws

Since the 2017 publication of the medical device regulation (MDR) and the IVD regulation (IVDR), EU regulations for medical ...
Business Wire

First Global Regulatory Standards for “Single-Use” Medical Device Reprocessing and Remanufacturing Published by the Association of Medical Device Reprocessors

WASHINGTON & BERLIN--(BUSINESS WIRE)--When health systems and hospitals use regulated reprocessed “single-use” devices, they reduce procedure costs without compromising patient safety, build supply ...
PharmiWeb

2 Day Virtual Asia-Pacific Medical Device Regulations Training Course: Navigate Evolving Regulatory Frameworks with Confidence to Access High-Growth Global Markets (Nov 3rd ...

DUBLIN--(BUSINESS WIRE)--The "Medical Device Regulations in Asia-Pacific Markets Training Course (Nov 3rd - Nov 4th, 2025)" training has been added to ResearchAndMarkets.com's offering. With the ...