Technical articles
18/09/2025
Simplifying EUDAMED compliance: The role of collaboration and expertise
Led by Ackomas, in collaboration with manufacturers and regulatory experts, the Practical EUDAMED Guide simplifies regulatory obli
4/09/2025
Efor and Ackomas elevate partnership to support medical device compliance
Together with Ackomas, we ensure that medical device manufacturers can transition effortlessly into compliance mode, while also se
28/08/2025
FDA’s 2025 regulatory shift: integrating sex-specific data across the medical device lifecycle
In 2025, the FDA is enforcing a regulatory revolution: integrating sex-specific differences at every stage of the medical device l
14/08/2025
6 years of commitment and growth: Pauline’s inspiring journey at Efor
Efor has succeeded in fostering a caring company culture that highlights its talents.
7/08/2025
MDR 2017/745 and IVDR 2017/746: What requirements for what solutions?
This article delves into these regulatory expectations and provides essential insights for navigating this reinforced framework.
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31/07/2025
Efor completes third acquisition of the year with the integration of PES
Efor continues its targeted growth strategy with the acquisition of Process Engineering Specialists (PES), a well-established play
24/07/2025
ECHA accelerates the transition towards animal-free chemical evaluations
The ECHA is announcing its commitment to drastically reduce, and then eliminate, animal testing.
10/07/2025
Women in Engineering Day: Amandine’s story of leadership, resilience and technical excellence
Amandine Pousse shares her inspiring engineering journey on International Women in Engineering Day.
26/06/2025
Efor takes action for cancer research with the “Get Your Sneakers On” challenge
Our employees took part in the “Get Your Sneakers On” challenge organized by the Centre Léon Bérard.
24/06/2025
Efor strengthens its European presence with a new office in Frankfurt
Efor continues its international expansion with the opening of its first office in Frankfurt, Germany.
19/06/2025
Bioproduction 2030: Innovate, train, collaborate to build the future of biopharmaceuticals
Efor at the National Day of Bioproduction of Biopharmaceuticals.
12/06/2025
Lifetime and Lifecycle in the Upcoming ISO 10993-1 Standard (2025): Who, When, What, and How?
Analysis of the life cycle and service life of a medical device to better anticipate the challenges of biological evaluation under
