Efor news & technical articles
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
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
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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
