51ÁÔÆæ

In this soundbite from 51ÁÔÆæ Radio, Dr. Helin Raagel and Dr. Matthew Jorgensen from Nelson Labs explain why the Cytotoxicity test during a biocompatibility evaluation is the most important test...

Click now to listen to 51ÁÔÆæ's Susan Schniepp and Steven Lynn, in this 51ÁÔÆæ Radio audio update: Personalized Medicine Software as medical device (SaMD) continues to emerge in consumer products,...

The International Medical Device Regulation Forum (IMDRF) recently published updated cybersecurity guidance for the medical device industry. The medical device cybersecurity working groups at IMDRF have been busy lately, publishing...

The global pandemic and continued supply chain disruptions have prompted many U.S. pharmaceutical and medical device manufacturers to reassess their reliance on offshore production. As organizations place greater emphasis on...

Why has product launch become more complex after the pandemic & how have the "roots of compliance" changed the EU regulatory environment? In this sound bite from 51ÁÔÆæ Radio, host...

What should you do if you are having trouble executing your design protocols? Listen to this highlight from 51ÁÔÆæ Radio where Walter Mason explains what needs to be done if...