Article R1243-18
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…
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Showing 71–80 of 38628 articles for “Art. L 1243-11”
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…
Any organisation which ensures the conservation and preparation of tissues or cells from the human body and their derivatives, with a view to their transfer for scientific use, including for the purpo…
The declaration is made up of a letter signed by the legal representative of the applicant organisation and a supporting file, entered using a teleservice. The letter describes the activity and certif…
Subject to the provision of the second paragraph relating to blood establishments, the establishment or authorised body shall set up a scientific council or a medico-technical committee, responsible i…
To avoid any risk of cross-contamination, when activities involving the preservation, preparation and transfer for scientific purposes of tissues or their derivatives or of cells are carried out on th…
A copy of the complete dossier is sent by the Director General of the Agence nationale de sécurité du médicament et des produits de santé to the Director General of the Agence de la biomédecine. The D…
Any change in the information contained in the declaration file that is likely to result in a substantial change in the conditions under which the declared activities are carried out, in particular a…
The dossier is deemed to be complete if, within one month of receipt, the Minister responsible for research or, where applicable, the Director General of the regional health agency, has not informed t…
For the application of the provisions of sub-sections 1 to 4, army hospitals and the army blood transfusion centre shall be considered as health establishments and a blood transfusion establishment re…
The application is deemed to be complete if, within one month of receipt, the Minister responsible for research or, where applicable, the Director General of the regional health agency, has not inform…
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