Technical articles
3/04/2025
International Women’s Rights Day
Looking back on our solidarity challenge for International Women's Rights Day.
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
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.
30/05/2024
Shared audits: a simple, cost-effective solution for suppliers, subcontractors and service providers
Suppliers, subcontractors and service providers are increasingly called upon by their customers to carry out assessment audits. Th
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
Join our team
Consult our offers
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
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
19/10/2023
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
17/10/2023
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.
22/06/2023
Quality of Work Life Week at Efor
From June 19 to 23, it was the Quality of Work Life Week!!
