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Showing 841–850 of 4251 articles for “Art. 20 Mar 2019”
On a proposal from the Director General of the Agence nationale de sécurité du médicament et des produits de santé, the following are set: 1° By order of the Minister for Health: a) The maximum doses…
…eterinary medicinal products mentioned in this article, the dossier attached to the application for marketing authorisation is compiled under the following conditions by way of derogation from the fir…
All acts relating to the activities mentioned in Article R. 5142-1 or Article R. 5142-40 are carried out under the effective control of a pharmacist or a veterinarian who meets the conditions for prac…
The labelling of a medical device given to the end user or patient, the accompanying leaflet and any other information relating to its operation or use must include a version written in French.
The manufacturer may instruct his authorised representative to initiate the procedures mentioned in 1°, 2°, 4° and 5° of article R. 5221-19.
When informed of one of the events mentioned in Article L. 5212-2, the Director of the Agence nationale de sécurité du médicament et des produits de santé (French National Agency for the Safety of Med…
…reusable in such a way as to allow aggregation. To this end, any person who places products on the market within the meaning of Article L. 5232-5 shall make the information available either on a dedi…
…ronic signature has been affixed in accordance with the provisions of the aforementioned Decree No. 2017-1416 of 28 September 2017.
The establishment organises the referral of patients who do not require treatment by the emergency department to another care structure or to a social or medico-social structure, in accordance with pr…
The National Committee makes its decisions on the basis of applications. Project promoters are heard by the rapporteur at their request. They may also be heard by the relevant section of the National…
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