News Efor
12/12/2024
Efor Recognized Among the Great Place to Work Switzerland 2024
Efor recognized among Switzerland's top employers with its Great Place to Work 2024 nomination.
28/11/2024
CDISC: Towards successful clinical trials!
In clinical research, data management and analysis are of fundamental importance in guaranteeing the validity and reliability of r
21/11/2024
Stability and transport validation of sterile medical devices
Validating the stability and transport of sterile medical devices is an essential process for ensuring the safety and efficacy of
14/11/2024
EFOR strengthens its social commitment by signing the ProMilès Manifesto
EFOR strengthens its commitment to military career transitions with the ProMilès Manifesto.
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
31/10/2024
Medical and scientific communication: disseminating knowledge for the benefit of patients and practitioners
Manufacturers use ever-more-innovative technology to provide items at the forefront of medical research, contributing to the desig
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
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
7/08/2024
Importance and design of PMCF studies for medical devices in Europe: framework and principles
Medical Device Regulation (MDR) 2017/745, which has been enforced since May 26, 2021, has significantly reinforced the regulatory
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
