Learn more about Assent's platform solution for supply chain data management.
Learn how to meet new EU Medical Device Regulation requirements to maintain market access, and certify in-scope products before the deadline.
Join Assent’s EU MDR experts as they explain what the EU MDR means for companies and what steps can be taken to bring older devices into compliance.
Join Bruce Jarnot as he discusses how to update your compliance program to collect new product information and meet the TSCA deadlines.
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