Efor news & technical articles
Technical Management Seminar: a look back at an event like no other
Retour sur un évènement phare : le séminaire de la Direction Technique
Ensuring the safety of medical devices, an essential tool: risk management according to ISO 14971:2019
IntroductionMedical Devices (MD) and In Vitro Diagnostic Medical Devices (IVDMD) shall be designed and manufactured to ensure thei
Nodarius joins the Efor Group: A new alliance for a shared vision
The Nodarius Group joins the Efor Group to build on its ambition to become a world leader
Metagenomics is a method for studying the microbiome, i.e., all the microorganisms (bacteria, viruses, fungi, yeasts, plankton, et
Efor accelerates the structuring of its center of excellence for health data valorization.
With a position among the leaders in specialized consulting for Life Sciences industries, the Efor Group supports its clients thro
ICH Q12 application for the implementation of a change: example of a site transfer
The ICH Q12 guideline entitled « Technical and regulatory considerations for pharmaceutical product life cycle management” is
Efor X Institut Pasteur de Dakar
We are delighted to announce that Efor has entered into a collaboration with the Institut Pasteur de Dakar to support its major ex
Committed to Pink October! 🎗️
At Efor, we are proud to commit ourselves to a cause that is particularly close to our hearts: raising awareness for breast cancer
Proud to have run for cancer research!!
A group of our Eforcenes took part in the charity run organized by the Leon BERARD center this Sunday.
Clinical evaluation according to Article 61(10) of Medical Device Regulation (EU) 2017/745
Purpose of conducting a clinical evaluationRegulation (EU) 2017/745 (article 2(44)) relating to medical devices defines clinical e
Toxicological risk assessment and 2023 revision of ISO 10993-17 standard
All the answers about ISO 10993-17 and its revision