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Medical Device Courses

Academy Representative 844-488-8872

*NEW* New Regulation for Medical Devices (EU) 2017/745 MDR: for Manufacturers/ Technical Documentation

MDD to MDR Transition

MERCOSUR

MDSAP Overview

New Regulation for Medical Devices (EU) 2017/745 MDR: General Introduction and Principles. Special requirements for Distributors and Importers

ISO 13485:2016 Understanding the Requirements

ISO 13485:2016 Internal Auditor

MDSAP Internal Auditor

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Academy Coordinator

844-488-8872 Option 5

academy-us@tuv-nord.com