April 16, 2019 By Danielle Kirsh Egypt fast-track medical device registration pathway speeds up market access timeframes
April 12, 2019 By Danielle Kirsh Canadian regulators clarify changes in qualifications for medical device licenses following Sterigenics shutdown
April 10, 2019 By Danielle Kirsh FDA identifies hundreds of device types affected by sterilization facility closures
April 8, 2019 By Danielle Kirsh FDA recommendations from the annual Human Factors and Ergonomics Society symposium
March 26, 2019 By Danielle Kirsh FDA reviews requirements for nicotine replacement therapy product labels
March 25, 2019 By Danielle Kirsh Dutch regulators explain no-deal Brexit impact for medical device companies
March 21, 2019 By Danielle Kirsh Taking a more rigorous approach to investigating fatal medical errors in the U.S.
March 15, 2019 By Danielle Kirsh Australia medical device regulators prepare Brexit contingency plans