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Showing 8721–8730 of 51804 articles for “Art. L 225-3”
The prescription is validated within a maximum of fifteen days of receipt.Within a maximum period of three months following validation of the pathway prescription by the designated structure, the chil…
These registers must be kept in premises close to those where gametes, germ tissue or embryos are stored, under conditions that ensure confidentiality.
To facilitate the performance of the responsible person's duties, agreements are concluded between the structures authorised to carry out one or more clinical activities in medically assisted procreat…
The rules of good practice applicable to ovarian stimulation, including when it is carried out independently of a medically assisted procreation technique, are set by order of the Minister for Health,…
Practitioners meeting the criteria mentioned in article R. 2142-11 for the conservation of gametes, germinal tissue or embryos are responsible for keeping the registers mentioned in articles R. 2142-3…
Any incident or adverse reaction occurring during the import or export operation and likely to affect the quality or safety of gametes or germ tissue must be reported to the person referred to in 6° a…
Any import or export of gametes or germinal tissue is subject to the following information being affixed to the external packaging, in addition to the information mentioned in 4° to 7° of Article R. 2…
Where the Director General of the Agence de la biomédecine finds that the requirements laid down in the import or export authorisation have not been complied with, he may immediately suspend the autho…
The gamete, germinal tissue and embryo registers provided for in articles R. 2142-33 and R. 2142-34, as well as, where applicable, the information mentioned in article R. 1244-5 concerning the gamete…
Repeated offences under articles R. 2222-1 and R. 2222-2 are punishable in accordance with article 132-11 of the French Penal Code.
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