Efor news
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
23/10/2025
IT Infrastructure Qualification: Better Risk Management Due to Regulatory Requirements
The qualification process—covering IQ, OQ, and PQ—takes a structured and thorough approach to validating technical components
16/10/2025
Efor recognized in the 2025 Décideurs Innovation ranking
Efor has been recognized by Décideurs Innovation in their 2025 ranking dedicated to the Health, Pharmacy, and Biotechnology se
9/10/2025
Understanding and mastering the differences between clinical evaluation and clinical investigation of medical devices
The distinction between clinical investigations and clinical evaluations is crucial, yet the two terms are still too often confuse
9/10/2025
Efor wins the Grand Prix des Lionnes 2025
Efor, winner of the Grand Prix des Lionnes in the Business Services category.
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2/10/2025
South-west: a new chapter for Efor in Toulouse
Our Toulouse teams had the pleasure of moving into their brand-new offices in the heart of the Vidailhan eco-district in Balma.
25/09/2025
The evolution of the european regulatory framework regarding electronic instructions for use (EIFU) of medical devices: analysis of regulation (EU) 2025/1234 amending regulation (EU) 2021/2226
Since the adoption of Regulation (EU) 2017/745 on Medical Devices, the European Commission has embarked on a modernization effort
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
11/09/2025
CLP, REACH and PPWR: Toward Strategic Regulatory Convergence to Support Sustainable Innovation in Life Sciences
The European Union (EU) is undergoing a major overhaul of its strategy on chemical safety, product traceability and environmental
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.
