Technical articles
7/11/2024
Julie Marion featured on Pharma Minds: a powerful conversation on the future of the pharma industry
Julie Marion, Co-Founder and Chief Operating Officer of Efor, had the honor of being a guest on Pharma Minds, a must-listen podcas
24/10/2024
Efor inaugurates its new offices in Bordeaux!
At Efor, we are proud to share exciting news: the opening of our brand-new offices in Bordeaux!
17/10/2024
Management of user interfaces of unknown provenance (UOUP) in medical devices according to the IEC 62366-1:2015 + A1:2020 standard
With the implementation of European Regulation (EU) 2017/745, both the official texts and the authorities are placing particular e
27/09/2024
ISO/DIS 10993-1, A new revision underway – Analysis of the ISO 10993-1 standard revision draft
The draft of the new revision of ISO 10993-1, addressing the biological evaluation of medical devices (MD), was released at the en
18/07/2024
Efor celebrates one year of partnership with RAISE’s “Investir pour l’Enfance”
It’s been a year since we integrated RAISE’s “Investir pour l’Enfance” philanthropic fund into our c
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9/07/2024
Efor : Developing HR skills internationally
At Efor, we firmly believe that continuous training is an essential lever for growth and innovation. With this in mind, on June 19
2/07/2024
Medical Devices: Now Introducing the Medical Visit Charter!
The Medical Device (MD) and In Vitro Diagnostic Medical Device (IVDMD) sector is subject to increasingly stringent regulations.
2/07/2024
Quality of Life at Work Month at Efor: A commitment to employee well-being
At Efor, we firmly believe that the well-being of our employees is essential to their personal and professional development. With
28/06/2024
Efor : Committed to Health and Well-being with the “À Vos Baskets” Challenge
At Efor, the health and well-being of our employees is a core concern. As part of our Corporate Social Responsibility (CSR) policy
16/05/2024
Regulatory and Standard Monitoring: Staying the Course Towards Compliance
Whether in the life cycle of a medical device (MD) or an in vitro diagnostic medical device (IVDMD), it is not uncommon to face un
17/04/2024
Focus on AET and TSL
Among the changes introduced by the 2023 version of ISO 10993-17 (Biological evaluation of medical devices - Toxicological risk as
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
