Simplifying Global Compliance
Featured Product In Quality
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
Quality
EU MDR Compliance: A Checklist for Meeting Manufacturing, Safety and Performance Requirements
$397.00
Meeting the Competence, Training and Awareness Rules for Medical Device Manufacturers - Webinar Recording/Transcript
$287.00
Medical Device Calibration: A Step-by-Step Guide to Meeting FDA and ISO Standards
$197.00
Setting and Measuring Quality Objectives for Medical Devices - Webinar Recording/Transcript
$287.00