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Showing 3301–3310 of 20753 articles for “Art. CA Paris 13-6-2024 n° 22/08263”
…on the list set out in Annex II to the aforementioned Delegated Regulation, after a risk of falsification has been identified.
…n of the medicinal product notifies the Director General of the Agence nationale de sécurité du médicament et des produits de santé of the batch number of the medicinal product being distributed, stat…
…report to the marketing authorisation holder for this proprietary medicinal product and, where applicable, to the company or organisation responsible for the operation of the proprietary medicinal pro…
All medicinal products are fitted with the tamper-evident device referred to in Article R. 5121-138-2. However, this device is not compulsory for medicinal products on the list set out in Annex I to C…
I.-The outer packaging or, where there is no outer packaging, the immediate packaging of medicinal products bears safety features consisting of a unique identifier and a tamper-evident device, under t…
…city, identify and provide proof of unlawful handling of the medicinal product. This replacement is carried out without opening the immediate packaging as defined in 3° of article R. 5121-1 and in com…
…nal health agency and the president of the competent conseil de l'ordre of this dissolution. In all cases of dissolution, the liquidator will inform them of his appointment. To this end, he shall send…
The Regional Committee for Employment, Vocational Training and Guidance will set up the committees necessary for its operation, as well as a permanent secretariat.
Without prejudice to the application of the provisions of articles R. 6332-5 to R. 6332-7, the authorisation referred to in article R. 6523-2-9 is revoked, by joint order of the ministers responsible…
…here a veterinary medicinal product, which has already been authorised or is the subject of an application for marketing authorisation under examination in another Member State of the European Union,…
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