by Tim Bubb | Nov 29, 2022 | Clinical Writing, IMed Consultancy, IVD, MDR, Medtech Marketing, PMS
New FDA Software Guidance Published to Help Developers Identify if their Software is considered a Medical Device in the USA. STAY IN THE KNOW Sign up to get the latest updates. Don't worry.... we don't like spam either Success! Name Email Subscribe FDA has recently...
by Leeanne Baker | Feb 28, 2019 | PMS, Usability
How your Post Market Surveillance data can help you with the usability of your established medical device STAY IN THE KNOW Sign up to get the latest updates. Don't worry.... we don't like spam either Success! Name Email Subscribe Usability of medical devices is a hot...
