Home     |     Our Team     |     News     |     Contact Us     |     Call: 508-231-8842

Document Repository

Just wanted to remind you about the documents that are available to download in the Document Repository; please click here to get to the Document Repository. Design Verification Design Verification: This paper explores the use and misuse of Design Verification and how...

News and Resources

RAPS Euro Convergence 2020 Summary

RAPS Euro Convergence 2020 Summary

The 2020 conference, or “convergence,” of European regulatory professionals that was originally to be held in October in Brussels instead took place virtually due to the pandemic. Even though it was conducted entirely online, the convergence covered a lot of...

read more
Person Responsible for Regulatory Compliance

Person Responsible for Regulatory Compliance

As the European Union’s (EU) Medical Device Regulation (MDR) and In-Vitro Diagnostic Medical Device Regulation (IVDR) continue to evolve, one requirement is getting a lot of attention – the person responsible for regulatory compliance (PRRC). This individual (or...

read more

Contact Us

MEDIcept

Main Office

200 Homer Ave
Ashland, MA 01721

508-231-8842