https://www.intertek.com/assurance/mdr/
MDR Certification | EU Medical Device Regulation 2017/745
Get MDR compliance certification through Intertek Medical Notified Body (NB 2862). Expert support for medical device transition deadlines, clinical data, and...
eu medical device regulationmdrcertification2017745
https://kpmg.com/us/en/capabilities-services/our-healthcare-and-life-sciences-capabilities/eu-mdr-advisory-services.html
EU Medical Device Regulation (MDR) Advisory Services
EU MDR regulation officially published May 5, 2017 triggered a formal implementation and transition timeline. KPMG can help.
eu medical device regulationmdradvisoryservices
https://www.bsigroup.com/es-ES/training-courses/eu-medical-device-regulation-mdr-2017745-qms-auditor-international-training/
EU Medical Device Regulation (MDR) 2017/745: QMS Auditor | BSI
This course is designed to give you insights into how Notified Bodies may perform an MDR QMS compliance audit, using the topics of a typical MDR audit agenda...
eu medical device regulationmdr2017745qms
https://www.bsigroup.com/nl-NL/training-courses/eu-medical-device-regulation-mdr-2017745-qms-auditor-international-training/
EU Medical Device Regulation (MDR) 2017/745: QMS Auditor | BSI
This course is designed to give you insights into how Notified Bodies may perform an MDR QMS compliance audit, using the topics of a typical MDR audit agenda...
eu medical device regulationmdr2017745qms