Technical articles
6/11/2023
ICH Q12 application for the implementation of a change: example of a site transfer
The ICH Q12 guideline entitled « Technical and regulatory considerations for pharmaceutical product life cycle management” is
24/10/2023
Efor X Institut Pasteur de Dakar
We are delighted to announce that Efor has entered into a collaboration with the Institut Pasteur de Dakar to support its major ex
21/09/2023
Relocation of our Norman Agency
After Grenoble, it's now the turn of our Norman agency located in Val de Reuil to change environment and move into their new premi
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!!
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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 ...
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
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
