Article R5121-138-1
…compulsory prescription shall be provided with the unique identifier referred to in Article R. 5121-138-2, unless they are exempt from this requirement due to their presence on the list established in…
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Showing 4331–4340 of 5097 articles for “Art. 13”
…compulsory prescription shall be provided with the unique identifier referred to in Article R. 5121-138-2, unless they are exempt from this requirement due to their presence on the list established in…
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…
…f a unique identifier and a tamper-evident device, under the conditions set out in articles R. 5121-138-1 and R. 5121-138-3. II.-The unique identifier allows persons whose activity is the wholesale di…
The safety features may only be replaced by equivalent safety features in order to verify the authenticity, identify and provide proof of unlawful handling of the medicinal product. This replacement i…
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,…
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