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Showing 801–810 of 19581 articles for “Art. 21 mars 2001 + Cass. 3e civ.”
Decisions to authorise or withdraw authorisation taken in application of Article L. 1161-5 are published on the Agency's website. Decisions to withdraw programme authorisation may be accompanied by an…
Blood establishments, health establishments and health cooperation groups authorised to store labile blood products intended for therapeutic use must have a procedure for withdrawing any unit of such…
In blood establishments, venous blood samples taken from the elbow and capillary blood samples taken from a donor may be taken, under the direction and responsibility of the doctor mentioned in articl…
The Director General of the Agence de la biomédecine shall forward to the Minister for Research, within the time limit laid down in Article R. 1232-18, as necessary, any information revealing that the…
Implementation of the protocol is suspended or prohibited if the conditions that justified its authorisation are no longer met and after the establishment or organisation has been invited to present i…
An analytical accounting system covering the economic, financial and accounting data relating to the activities mentioned in article R. 1243-1 is set up within the establishment or authorised body.
Manufacturers of in vitro diagnostic medical devices may procure tissues, their derivatives and cells from the human body, whatever their level of processing, in a Member State of the European Union o…
The Director General communicates the Agency's opinions and recommendations to the ministers responsible for agriculture, consumer affairs, the environment, health and labour, as well as to the other…
The Prefect forwards the file, together with all the opinions received, to the Regional Prefect.
I.-The person responsible for the nuclear activity shall declare to the competent authority any significant radiation protection events, in particular :1° Events leading or likely to lead to significa…
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