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Showing 5841–5850 of 49555 articles for “Art. L. 125-5 V + jurisprudence”
For investigational medicinal products, the documents relating to each batch are kept by the pharmaceutical establishment which manufactures it, for at least five years after the end of the trial or t…
For each representative, an alternate is appointed under the same conditions as the full member. Alternates may attend meetings of the Regional Employment, Training and Vocational Guidance Committee w…
Regional cross-industry joint committees cannot be designated as operators of professional development advice by France Compétences.
Persons who complete a vocational training course for which the prison administration is responsible outside the institution under a semi-liberty or work release scheme are entitled to the remuneratio…
…orresponds to the number of units appearing in an initial outer packaging that complies with the provisions of article R. 5121-138, when the pharmacist dispenses the last units appearing therein, they…
In the event of agreement within the coordination group, referred to by the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail or by ano…
Any wholesale distributor, where he is not the marketing authorisation holder, who imports a veterinary medicinal product from another Member State shall inform the marketing authorisation holder and…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé may grant, under the conditions laid down in Article R. 5211-55 and Article 4 of Implementing Regulation…
…y checks that the authorised body has the required skills and up-to-date knowledge of the medical devices and active implantable medical devices manufactured from tissues of animal origin mentioned in…
Notwithstanding the provisions of Article R. 5222-18-4, where the second-hand in vitro diagnostic medical device which is the subject of the transfer has never been put into service, the file consists…
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