Technical articles
5/06/2025
Designing a PMCF Study: The Question of Sample Size with a Fictional Example
PMCF studies are key tools for meeting MDR requirements and ensuring device safety and performance.
28/05/2025
Efor Metz: a new workspace to support our growth
Efor Metz team has officially moved into their new office located at 1 rue Antoine Chaptal.
22/05/2025
The Impact of Presidential Executive Orders on the Pharmaceutical and Medical Devices sectors in the USA
Recent developments in United States (US) healthcare regulation have brought significant changes to the process of approving pharm
7/05/2025
Heading to North America
2025: A milestone in our international growthBringing together PharmEng Technology, Project Delivery Partners, and EFOR in 2025 ma
30/04/2025
Design and Development Management of a MD / IVDMD according to Standard EN ISO 13485:2016 + A11:2021
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24/04/2025
Efor signs the ProMilès Manifesto and extends its commitment across the entire group
Efor signe le manifeste ProMilès et étend son engagement pour la réinsertion des anciens militaires à toutes ses entités, en
17/04/2025
Team-building day for our CSR ambassadors
Last week, our CSR ambassadors gathered in Lyon for a meaningful moment of sharing, cohesion, and commitment.This meeting was a wo
10/04/2025
In-House Medical Devices: Understanding the Regulatory Framework and Compliance Requirements under European Regulations (EU) 2017/745 and 2017/746
This article explores the specific rules for so-called 'in-house' medical devices, manufactured or modified by healthcare institut
13/03/2025
Indications, Intended Purpose, Claims, and Medical Device Regulation 2017/745:What Are the Differences, and What Are the Implications?
In the field of medical devices, the terms indications, claims, and intended purpose/intended use play a fundamental role in the d
6/03/2025
Business Managers & Talent Acquisition Seminar: where performance meets solidarity
A look back at our annual Business Managers and Talent Acquisition seminar, which this year turned into a solidarity challenge.
27/02/2025
EN ISO 13485: 2016 / A11: 2021: The Strategic Lever to Transform Compliance into Competitiveness
ISO 13485 positions itself as an essential tool to protect patients and users while strengthening their confidence in medical devi
14/02/2025
Looking Back at the Technical Division Seminar
Efor’s Technical Division gathered in Ardèche, France for a new edition of its annual seminar.