Glossary entry (derived from question below)
English term or phrase:
MDD
French translation:
directive DM / directives relatives aux dispositifs médicaux
Added to glossary by
Moukhamadou Mansour Sine
Dec 28, 2023 09:47
4 mos ago
23 viewers *
English term
MDD
English to French
Medical
Medical: Cardiology
étude clinique, stents
Performed under: MDD
CIV ID or single identification number: Not applicable.
Clinical trials database reference and link:
ClinicalTrials.gov identifier NCT02276313
Je ne pense pas que "Major Depressive Disease" soit pertinent ici
CIV ID or single identification number: Not applicable.
Clinical trials database reference and link:
ClinicalTrials.gov identifier NCT02276313
Je ne pense pas que "Major Depressive Disease" soit pertinent ici
Proposed translations
(French)
3 +2 | directive DM / directives relatives aux dispositifs médicaux | Moukhamadou Mansour Sine |
Change log
Dec 29, 2023 19:23: Moukhamadou Mansour Sine Created KOG entry
Proposed translations
+2
26 mins
Selected
directive DM / directives relatives aux dispositifs médicaux
It could mean in this context Medical Devices Directive
The Medical Device Directive — Council Directive 93/42/EEC of 14 June 1993 concerning medical devices — is intended to harmonise the laws relating to medical devices within the European Union. The MD Directive is a 'New Approach' Directive and consequently in order for a manufacturer to legally place a medical device on the European market the requirements of the MD Directive have to be met. Manufacturers' products meeting 'harmonised standards'[1] have a presumption of conformity to the Directive. Products conforming with the MD Directive must have a CE mark applied. The Directive was most recently reviewed and amended by the 2007/47/EC and a number of changes were made. Compliance with the revised directive became mandatory on 21 March 2010.
The Medical Device Directive — Council Directive 93/42/EEC of 14 June 1993 concerning medical devices — is intended to harmonise the laws relating to medical devices within the European Union. The MD Directive is a 'New Approach' Directive and consequently in order for a manufacturer to legally place a medical device on the European market the requirements of the MD Directive have to be met. Manufacturers' products meeting 'harmonised standards'[1] have a presumption of conformity to the Directive. Products conforming with the MD Directive must have a CE mark applied. The Directive was most recently reviewed and amended by the 2007/47/EC and a number of changes were made. Compliance with the revised directive became mandatory on 21 March 2010.
4 KudoZ points awarded for this answer.
Comment: "Merci à tous"
Reference comments
1 hr
Reference:
see
Medical Devices Directive
https://www.bsigroup.com/globalassets/meddev/localfiles/fr-f...
They will also
facilitate the management of clinical investigations conducted under the Medical Devices Directive (93/42/
EEC) (MDD) or Active Implantable Medical Device Directive (90/385/EEC) (AIMDD), but continuing under the
Medical Device Regulation (2017/745) (MDR), or
https://www.bsigroup.com/globalassets/meddev/localfiles/fr-f...
They will also
facilitate the management of clinical investigations conducted under the Medical Devices Directive (93/42/
EEC) (MDD) or Active Implantable Medical Device Directive (90/385/EEC) (AIMDD), but continuing under the
Medical Device Regulation (2017/745) (MDR), or
Discussion