Publications : Medical devices

MDCG 2022-10 : Q&A on the interface between Regulation (EU) 536/2014 on clinical trials for medicinal products for human use (CTR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR)

Theme Clinical trials using diagnostic tests Target Audience Manufacturers and clinical trials sponsors Products concerned IVD & medicines Documents mentioned Regulation (EU) 2017/746 Regulation (EU) No 536/2014 Directive 98/79/EC   This guide provides...

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MDCG 2022-8 : Regulation (EU) 2017/746 – application of IVDR requirements to ‘legacy devices’ and to devices placed on the market prior to 26 May 2022 in accordance with Directive 98/79/EC

Theme Transitional provisions Target Audience Manufacturers, Authorised representatives, Importers, Distributors, Notified Bodies Products concerned IVD Documents mentioned IVDR (EU) 2017/746 IVDR – Article 110 Blue Guide MDCG 2019-5 MDCG 2021-13 rev.1   This...

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Christophe Claudon

After more than 20 years in medical device industry (manufacturing, quality and regulatory), I have started my new nexialist challenge in February 2022 as Quality Consultant with one main focus “THE PATIENT”, thus product safety. I worked for medical device supplier...

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Amina Mlaiki

Graduated from a multidisciplinary course in Sport Ergonomics and Motor Performance at the Faculty of Sport Sciences of Luminy. I am currently in Master 2 Bio-Engineering of Tissues and Implants. As part of my end-of-study internship, I am joining Nexialist for a...

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Séverine Gossé

I joined nexialist in July 2016, after several years of experience in tourism and as a small business manager. Today, my experience and knowledge benefit nexialist’s team. I mainly assist administrative and financial work as well as management and organization. It is...

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Saveria Dormenval

I joined nexialist on April 01, 2021 after 3 years of experience in the field of medical devices. I graduated as a biomedical engineer (ISIFC) in 2017 and then worked as a certification and validation engineer for an active medical device. I have developed skills on...

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