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Showing 1311–1320 of 5368 articles for “Art. 13 juill. 2010”
A claim for compensation for damage attributable to a preventive, diagnostic or therapeutic procedure or to a research procedure involving the human person shall be submitted to the Commission within…
Only medicinal products which have obtained a marketing authorisation issued by the European Union in application of Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 Mar…
I - Prior to any removal or collection of elements and products of the human body for therapeutic purposes from a living or deceased person, doctors and, in the situation referred to in IV, midwives e…
Any blood establishment collecting blood and its components, which prepares labile blood products intended for the preparation of intermediate products or medicinal products derived from blood, is req…
Revenue and imprest accounts may be set up under the conditions set out in Decree no. 2019-798 of 26 July 2019 on the revenue and imprest accounts of public bodies.
The provisions of articles R. 1242-6 and R. 1242-7 are applicable to cell harvesting activities authorised under this section.
The person in charge referred to in Article R. 1243-12 and the interim persons in charge, as well as the person in charge of activities, shall hold diplomas entitling them to practise medicine or phar…
The Director General of the Agence de la biomédecine shall take all necessary measures to guarantee the security and confidentiality of all nominative information contained in the register, in accorda…
The health establishments mentioned in the third paragraph of article L. 1233-1 which are not authorised to remove organs define, by means of an agreement with the establishments authorised to carry o…
By way of derogation from articles R. 1241-9 to R. 1241-12, when the removal of haematopoietic cells collected from bone marrow is envisaged from a minor for the benefit of one of his or her parents,…
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