We provide you with advice and expertise for the implementation of clinical studies, from the development of protocols (standard or innovative) to study reports, including all the follow-up stages.
At each stage, flexibility and rigor remain our priority.
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. [...]