60 mins

An Introduction to Medical Device Validation – Part 3

EU Medical Device Regulation (EU MDR) – Chapter 3: Identification, Traceability and Registration of Devices

An Introduction to Medical Device Validation – Part 2

EU Medical Device Regulation (EU MDR) – Chapter 2: Making Available on the Market

China Food and Drug Administration’s (CFDA’s) – GMP for Implantable Medical Devices

EU Medical Device Regulation (EU MDR) – Chapters 6 to 10

China Food and Drug Administration’s (CFDA’s) – GMP for Medical Devices

EU Medical Device Regulation (EU MDR) – Chapters 1 to 5

EU Medical Device Regulation (EU MDR) – Introduction

ISO 13485:2016 – Chapter 4: The Quality Management System (QMS)