Efor news & technical articles

6/02/2025
Efor strengthens its global ambitions with the acquisition of Project Delivery Partners
These acquisitions enhance our ability to deliver exceptional expertise to our clients while broadening our international footprin

30/01/2025
Ethylene Oxide: A Widely Used but Controversial Sterilizing Agent
La stérilisation à l’oxyde d'éthylène (OE) fait partie des méthodes les plus largement utilisées pour stériliser les disp

23/01/2025
Efor: Still Among the Leading Consulting Firms in Regulatory Affairs in 2024 🏆
Efor has once again been recognized as a “Leading” consulting firm in regulatory affairs...

16/01/2025
A Look Back at 2024: A Defining Year for Efor
The year 2024 has been much more than a series of achievements; it has been a collective journey marked by meaningful projects and

9/01/2025
A strategic alliance: PharmEng Technology joins the Efor group
We are proud to announce the acquisition of PharmEng Technology, a renowned Canadian company recognized for its expertise in valid

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20/12/2024
The Use of Artificial Intelligence in Omics to Predict Patient Survival
In recent years, artificial intelligence (AI) has been a highly publicized field due to its transformative impact on society. AI i

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

19/11/2024
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

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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

15/10/2024
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