Article R7343-26
…Autorité des relations sociales des plateformes d'emploi shall publish the list of admissible applications on the website provided for in Article R. 7343-10 fifteen days after expiry of the applicati…
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Showing 621–630 of 7791 articles for “Art. CA Paris – 26 June 2019 – no. 16/23435”
…Autorité des relations sociales des plateformes d'emploi shall publish the list of admissible applications on the website provided for in Article R. 7343-10 fifteen days after expiry of the applicati…
…anaging the in-house pharmacy is the recipient of all prescriptions drawn up in the context of home care provided to patients by the health care establishment. He organises for each patient, on the ad…
In the case provided for in article R. 5127-18, the public prosecutor notifies the interested party that the single sample is to be submitted for expert examination and informs him that he has three c…
List I medicinal products are kept in locked cabinets or premises containing nothing else, with the exception of dangerous substances classified as very toxic or toxic, in application of article L. 51…
…for Health made on a proposal from the Director General of the Agence nationale de sécurité du médicament et des produits de santé and after obtaining the opinion of the Director General of the Agenc…
…le de sécurité sanitaire de l'alimentation, de l'environnement et du travail. The authorisation indicates, where applicable, whether the medicinal product is covered by the provisions of article L. 51…
Where the undertaking is operated by a company, the competent corporate body of that undertaking shall appoint, at the same time as the pharmacist or veterinary surgeon in charge and in order to repla…
…anufacturer or his authorised representative shall, for a period of at least five years and, in the case of implantable devices, at least fifteen years after the last copy of the product has been manu…
In application of Article L. 5212-1, the list of medical devices subject to compulsory maintenance, the list of medical devices subject to internal quality control and the list of medical devices subj…
…f this Chapter which apply to the devices under consideration. The manufacturer must submit an application for assessment to an authorized body, which must include technical documentation enabling the…
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