Efor news & technical articles
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
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
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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
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
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18/06/2024
How to conduct a metagenomics project
Metagenomics, the science of genetic analysis of microbial communities, i.e., all the microorganisms (bacteria, viruses, fungi, ye
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
22/05/2024
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
