Efor news
8/03/2024
International Women’s Rights Day: our female employees speak out
To mark International Women’s Rights Day, we are highlighting the inspiring careers of three of our female employees working
5/03/2024
Literature review: a key element in DM development
The design of a medical device is a complex stage, requiring in-depth knowledge of available technologies, unmet clinical needs, e
20/02/2024
Technical Management Seminar: a look back at an event like no other
Retour sur un évènement phare : le séminaire de la Direction Technique
15/01/2024
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
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14/12/2023
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
12/12/2023
Metagenomics
Metagenomics is a method for studying the microbiome, i.e., all the microorganisms (bacteria, viruses, fungi, yeasts, plankton, et
5/12/2023
The Excellence Academy: a commitment to excellence at Efor
Recruiting has become a crucial issue, but it’s only the first step. At Efor, we firmly believe that to succeed and flourish
14/11/2023
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
6/11/2023
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
24/10/2023
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
9/10/2023
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
