RQM+ Medical Device and In Vitro Diagnostic Blog

on 21 June 2021 | By Celeste Maksim, PhD, RAC, RQM+

on 21 October 2020 | By Nancy Morrison, RQM+

R&Q's August 2020 webinar focused on Economic Operators: Addressing the EU MDR and IVDR requirements head-on. In this follow-up blog post, our knowledgeable MDR and IVDR regulatory experts sat down to answer audience questions.

on 29 July 2020 | By Deven Hennon, R&Q

Although a lot has changed in our worlds since R&Q's December 2019 webinar focused on Solving the EU MDR Labeling Puzzle, the general requirements have stayed the same. In this blog post, our knowledgeable EU MDR regulatory experts sat down to provide some updates on a few more...

on 6 July 2020 | By Deven Hennon, R&Q

R&Q's May 2020 webinar focused on FDA Emergency Use Authorization (EUA) process and EU MDR Article 59 to release devices needed for prevention and treatment of COVID-19. In this blog post, our knowledgeable FDA and EU MDR regulatory experts sat down to provide answers to your...