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Showing 2121–2130 of 38473 articles for “Art. L 227-13”
At the time of each parallel distribution operation, the company responsible for the parallel distribution of the medicinal product notifies the Director General of the Agence nationale de sécurité du…
When an adverse reaction to a proprietary medicinal product is reported to a company responsible for its parallel distribution, the latter will forward this report to the marketing authorisation holde…
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…
When the dissolution of the société de participations financières de profession libérale de pharmaciens d'officine does not result in its removal from the roll of the ordre, the liquidator informs the…
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…
Where 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,…
I.- In the event of repackaging, the holder of a parallel import authorisation for a proprietary veterinary medicinal product shall notify the holder of the marketing authorisation for the proprietary…
I.- By way of derogation from the provisions of article R. 6123-87-1, a holder of a surgical oncology authorisation who has rare specific equipment included on a list drawn up by order of the Minister…
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