Technical articles
12/09/2024
Quality Management System Regulation (QMSR), the FDA’s new regulation applicable to medical devices: We explain it all!
The QMSR, published by the FDA, imposes new requirements on medical device manufacturers. Discover the key changes to comply with
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
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
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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
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
