NOS SERVICES
Nous vous apportons conseil et expertise pour la mise en place d’études cliniques, de l’élaboration de protocoles (standards ou innovants) aux rapports d’études, en passant par toutes les étapes de suivi.
A chaque étape, flexibilité et rigueur restent notre priorité.
NEWS
INVITE TO MDG 2021 – MEDGENERACTION
On October 7, 2021 will be held MDG 2021-MedGenerAction, the largest annual event dedicated to Regulatory Activities applied to Medical Devices, organized by MD24, brand of Thema – a Complife Group Company – for the training of Quality & Regulatory Affairs professionals [...]
COMPLIFE QUALITY CERTIFIED ISO 9001:2015
Always attentive to the quality of its business processes, Complife Group in July obtains two important awards that certifies the conformity of the company in the execution of microbiological and chemical analyses and in the provision of [...]
IVDR (EU) 2017/746 SPECIALISED COURSE
To be prepared for 26 May 2022, the date of full application of the Regulation Medical Devices – Diagnostics in Vitro, is a real need for professionals and companies, in the field of Regulatory Affairs. [...]
