Technical articles
5/03/2026
The Talc Debate: Health Risks and Controversies
A seemingly harmless natural mineral, talc has once again become the focus of a major public-health debate in 2025
6/11/2025
Thresholds of Toxicological Concern (TTC)
The toxicological risk assessment of a device’s constituents (ISO 10993-17) relies on data obtained either through chemical char
30/10/2025
A month of commitment and solidarity for Breast Cancer Awareness Month 🩷
Throughout October, during Breast Cancer Awareness Month, Efor’s employees united around a cause especially close to our hearts
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.
Join our team
Consult our offers
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.
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
3/04/2025
International Women’s Rights Day
Looking back on our solidarity challenge for International Women's Rights Day.
27/03/2025
PFAS in Medical Devices and Pharmaceuticals: What manufacturers need to know
PFAS can be released and accumulate in the environment. They also pose risks to human health.
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
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
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
