QSR
Device Complaint Management: A Practical Guide to Evaluating, Investigating and Reporting
$397.00
Risk Management for Drug and Device Manufacturers: A Guide to FDA Policies and Processes
$397.00
Auditing for Quality Manufacturing: Five Areas of Risk for Drug and Device Manufacturers
$397.00
Usability Engineering: How the Updated ISO 14971:2019 Changes Your Process – Webinar Recording/Transcript
$287.00
Top Customs and FDA Enforcement Issues for Imports of Pharmaceuticals, Biologics and Medical Devices – Webinar Recording/Transcript
$287.00
