
MDR (EU) 2017/745 – Practical Management of Regulatory Obligations
a practical approach to managing the regulatory obligations required by the MDR
ABSTRACT
This course provides a practical approach to managing the regulatory obligations required by the MDR, with a focus on responsibilities, documentation workflows, and the checks required throughout the supply chain. Particular attention is given to the most common issues identified during audits and inspections.
FORMAT
1-day course: updated overview plus practical case studies on responsibilities and documentation checks.
Would you like to host this course at your company?
Contact Us
You may be interested also in
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
4 hours
Medical Devices
4 hours
Medical Devices
4 hours
Medical Devices
4 hours
Medical Devices
4 hours
Medical Devices
4 hours
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
8 hours
Medical Devices
8 hours
Cosmetics
4 hours
Cosmetics
8 hours
Cosmetics
4 hours
Cosmetics
4 hours
Cosmetics
4 hours
Cosmetics
4 hours
Cosmetics
4 hours
Cosmetics
4 hours
Cosmetics
6 hours
Nutraceuticals
4 hours
Nutraceuticals
4 hours



















