EU Medical Device Regulation (EU MDR) with a focus on clinical investigations (Overview)
Regulatory
Description
The EU MDR went live on 26 May 2021. For European Member states it is the binding regulatory framework for managing the medical device lifecycle.Â
This training provides an overview of the EU MDR (2017/745) legal requirements, with a focus on Chapter 6 (clinical evaluation and clinical investigation).
Intended audience
Basic training for staff working in the Medical Devices Sector
Prerequisite training
None
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Training design
Recorded session
Training duration
75-90 min.
Training language
English
€ 50 pp ex. VAT
Trainer: D. Malisse
More than 20 years of experience in the pharmaceutical and devices industry, including more than 10 years in quality responsibility, where knowledge of regulations and ethics is key.
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