Technical articles
24/07/2023
Efor ranked as essential in regulatory affairs in Décideurs Magazine
📣We are pride to announce that the Efor Group is now ranked “Leading” in the field of regulatory affairs consu
8/06/2023
Grenoble is packing up and changing premises!
Welcome to the new premises of our Grenoble agency!!
29/05/2023
Efor becomes a patron of Centre Leon BERARD and commits to the fight against cancer
We are proud to announce that we are supporting the Leon BERARD cancer center.
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
11/02/2023
Efor US. is born
Before closing 2022 marked by growth, resilience and starting a new year rich in projects ...
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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
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
14/09/2022
Launching Virtual Reality Training Programs
Tree, the training center of the Efor Group, reinforces its expertise and innovation capacity through immersive virtual reality tr
9/08/2022
Advertising for medical devices (MDs / IVDMDs)
Since 1 January 2013, regulations on advertising have applied not only to pharmaceutical companies, but also to manufacturers of m
7/07/2022
DMDIV: Gradual implementation of regulation (EU) 2017/746
Since 26 May 2002, the placing on the European market of all IVDMDs has been subject to compliance with Regulation (EU) 2017/746 &
7/07/2022
MD marketing in the USA: what are the steps of the 510(k) submission procedure?
Why market a medical device in the United States?The USA is currently the largest medical device market, accounting for 45% of the
