Featured Product In Postmarket Safety
Biological Risk Evaluation and Management for Medical Devices
$397.00
Report shows how the FDA incorporates the two ISO standards in its medical device development policy, how the EU version of the two standards differs in significant ways and how the EU Medical Device Regulation may require further changes in the European standards. Read More
Postmarket Safety
Continuous Quality Improvement for Pharmaceutical and Medical Device Manufacturers – Webinar Recording/Transcript
$287.00
Using Monte Carlo Simulation to Aid Your Medical Device Design – Webinar Recording/Transcript
$287.00
FDA’s Regulation of Digital Health Wearables & Sensors – Webinar Recording/Transcript
$287.00
Usability Engineering: How the Updated ISO 14971:2019 Changes Your Process – Webinar Recording/Transcript
$287.00
