Efor news & technical articles
3/04/2023
MD: the role of pre-clinical data in technical documentation (MDR & ISO 13485 :2016)
Medical devices shall achieve the performance intended by their manufacturer and shall be designed and manufactured in such a way
1/03/2023
We broke records at the Eco Sport Challenge!
On March 18th, the Lyon-based Efor teams participated in a unique inter-company challenge with great enthusiasm: picking up as man
11/02/2023
Efor US. is born
Something is coming …Before closing 2022 marked by growth, resilience and starting a new year rich in projects, we are laun
7/02/2023
Extension of the Ecovadis Label
The Efor group reinforces its CSR approach and actions, as recognized by the extension of the silver medal awarded by Ecovadis. We
18/01/2023
Opening of the new Basel offices
Welcome in Basel !!!!Last week our teams met to inaugurate our new offices in Basel.It was the perfect opportunity for the Swiss t
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15/12/2022
How to implement the IEC 60601-1 standard when placing medical electrical equipment on the market
ScopeIEC 60601-1 is the umbrella safety standard for medical electrical (ME) equipment. As its name suggests, ME equipment re
12/12/2022
Efor X UTBM Partnership – Together for Telethon
Last December 1st, the Efor and UTBM Junior teams decided to join forces and energy to support the 2022 Telethon.The event include
30/11/2022
DM/DMDIV: Analysis and trend reports during post-marketing surveillance
The Medical Devices Regulations (MDR) 2017/745 and the In Vitro Diagnostic Medical Devices (IVDR) Regulation 2017/746 require the
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10/11/2022
Medical and scientific writing
Medical and scientific writing encompasses a range of writing activities in the areas of medicine and science, whether they focus
20/10/2022
Changes to medical devices (MDs / IVDMDs)
Once CE marked The life of a medical device is not a long, quiet river… Who has never attended a team meeting on a change t
4/10/2022
EU GMP Annex 1 update: what has changed, and what are the impacts?
EU GMP Annex 1 on good manufacturing practice defines rules for the manufacture of sterile medicinal products. Based on a 2008 ver
