Medical Device Webinars

-

Register in advance for one of our upcoming webinars featuring our medical device experts from around the world. We will discuss medical device-related regulations and standards, including the new Medical Device Regulation (MDR), In Vitro Diagnostic Device Regulations (IVDR), and ISO 13485:2016.

[insert timetable when ready and Pardot registration form?]

In Vitro Diagnostic Device Regulation (IVDR)

In Vitro Diagnostic Device Regulation (IVDR)

Find out if you are ready for the new IVDR

Прочетете повече
ISO 13485:2016 Certification

ISO 13485:2016

Your company could benefit from our ISO 13485:2016 services

Прочетете повече
In Vitro Diagnostic Device Regulation (IVDR)

Medical Device Single Audit Program (MDSAP) Certification

Certified once, recognised globally. Is the MDSAP for you?

Прочетете повече