June 25, 2019 By Danielle Kirsh LRQA to withdraw European Notified Body medical device and IVD manufacturers services
June 7, 2019 By Danielle Kirsh Human factors and usability investment considerations for medtech companies
May 30, 2019 By Danielle Kirsh India regulators list risk classifications for 12 notified medical devices
May 13, 2019 By Danielle Kirsh FDA issues final Q-Submission guidance to include medical device cybersecurity coverage
May 10, 2019 By Danielle Kirsh Canadian regulators recommend 3D-printed medical device license applicants
May 2, 2019 By Danielle Kirsh Latest Brexit extension raises more questions for U.K. and European medical device industries