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EU MDR Compliance: A Checklist for Meeting Manufacturing, Safety and Performance Requirements
$397.00
The FDAnews report EU MDR Compliance can help. Our editors have combed through the regulations, picking out the most minute compliance points and building them into a checklist of 200+ requirements you can use to confirm that you are satisfying all the EU mandates for device manufacturing. Read More
Quality
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
How to Deploy Root Cause & CAPA to Minimize Human Error – Webinar Recording/Transcript
$287.00
