Article R1131-18
The holder of the authorisation referred to in Article R. 1131-13 is required to declare to the competent regional health agency and to the Agence de la biomédecine, the names of the approved practiti…
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Showing 811–820 of 3891 articles for “Art. 18 Mar 1993”
The holder of the authorisation referred to in Article R. 1131-13 is required to declare to the competent regional health agency and to the Agence de la biomédecine, the names of the approved practiti…
When the condition of the person who has suffered damage has been consolidated after the date on which the Commission issued its first opinion, or when new damage attributable to a worsening of the pe…
The authorisation is issued for a period of three years and may be renewed for an identical period on application by the authorisation holder to the Director General of the Agence nationale de sécurit…
One or more samples of the biological product used to carry out the medical biology analyses provided for in articles R. 1211-14 to R. 1211-16 are kept under conditions set by order of the Minister fo…
The function of whole blood collection includes the actual collection operation and participation in monitoring its proper performance.Only the following may perform this function within a blood estab…
I.-The distribution and supply of labile blood products required by health establishments and health cooperation groups authorised to manage a blood depot are carried out by a single blood establishme…
Applicant establishments or organisations have the equipment described in the rules of good practice provided for in article L. 1245-6, enabling them to guarantee the quality, health safety and tracea…
Implementation of the protocol may begin on expiry of the two-month period following issue of the acknowledgement of receipt, unless the Minister responsible for research decides to prohibit implement…
I.-The Committee will issue a scientific, technical and ethical opinion within one month of the matter being referred to it. Committee members will assess the educational and scientific value of the p…
The Agence nationale de sécurité du médicament et des produits de santé has a period of four months to evaluate the information provided. At the end of these maximum four months, when, in application…
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