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
FDA Digital Health Regulation: Latest Developments for Medical Device Manufacturers – Webinar Recording/Transcript
$287.00
Medical Device Cybersecurity: Understand the Latest Developments – Webinar Recording/Transcript
$287.00
FDA Under the Biden Administration: What’s to Come and What It Will Mean – Webinar Recording/Transcript
$287.00
Spreadsheet Validation: Best Practices to Maintain Compliance – Webinar Recording/Transcript
$287.00
