September 9, 2019 By Danielle Kirsh Examining common medical device cybersecurity approaches in the U.S., Canada and Australia
September 3, 2019 By Nancy Crotti FDA requires more postmarket data to keep certain devices on the market
September 3, 2019 By Danielle Kirsh How medical device early-use research and testing affects product design and development
August 30, 2019 By Danielle Kirsh IMDRF publishes Conformity Assessment Body recognition requirements
August 29, 2019 By Halle Kirsh Webinar: Quality experts share keys to medical device design controls success
August 29, 2019 By Danielle Kirsh FDA finalizes post-market safety reporting guidance for combination products
August 26, 2019 By Danielle Kirsh FDA adds AAMI/UL 2800 standards for medical device interoperability