Article R5124-57-4
The importing pharmaceutical establishment shall ensure that the investigational medicinal products it imports have been subjected to standards of good manufacturing practice at least equivalent to th…
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Showing 3901–3910 of 26972 articles for “Art. CE 16-4-2012 n° 323592”
The importing pharmaceutical establishment shall ensure that the investigational medicinal products it imports have been subjected to standards of good manufacturing practice at least equivalent to th…
…representation of plastic, graphic or photographic works of art by automated image referencing services is based on the revenue from exploitation or, failing that, assessed on a flat-rate basis in the…
…those of the Board of Directors; 7° The general terms and conditions of sale for products and services provided by the establishment; 8° loans; 9° Acceptance or refusal of gifts and bequests; it may…
In the case of production, project development aid may not have the effect of bringing the total amount of public financial aid: 1° For feature-length cinematographic works and audiovisual works, to m…
…y information that would enable the donor and recipient to be identified. They shall ensure compliance with the provisions of article R. 1245-2.The legal or natural persons mentioned in the first para…
I.-The missions of the national centres of reference are :1° Expertise in the microbiology and pathology of infectious agents, the development, optimisation, validation and distribution of medical bio…
The local correspondent for the vigilance system relating to medically assisted procreation is responsible for : 1° Ensuring that the health professionals involved in the activities mentioned in 2° of…
…f approved civil security associations belong to the following categories: 1° Holders of the ambulance driver's state diploma instituted by the minister responsible for health; 2° Persons holding the…
…mentioned in that Article only if they meet the conditions set out in Articles 72a, 72b with the exception of point d of its paragraph 2 and 72c of Regulation (EU) No 575/2013 of the European Parliam…
…within the remit of the Agency. It also defines the criteria for assessing the training and experience required to approve the practitioners mentioned in 11° of the same article.In addition to its Cha…
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