Article R5126-101
A pharmacist covered by the provisions of article L. 4138-2 of the Code de la Défense, appointed by the Minister for Defence, manages the pharmacy for internal use of the pharmacie centrale des armées…
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Showing 1651–1660 of 38878 articles for “Art. al. 9 · Art. R 228-10”
A pharmacist covered by the provisions of article L. 4138-2 of the Code de la Défense, appointed by the Minister for Defence, manages the pharmacy for internal use of the pharmacie centrale des armées…
Whatever the cause and duration of the absence of the pharmacist in charge of the pharmacy for internal use, his replacement may not exceed one year. This replacement is carried out by a pharmacist co…
Health professionals, in application of the first paragraph of II of Article L. 5131-5: 1° Must report without delay to the Agence nationale de sécurité du médicament et des produits de santé any seri…
The samples taken are sealed. These seals are applied to a label containing the following information in particular: 1° The name of the product ; 2° The category to which the product belongs, with ref…
An order of the Minister for Health, issued on a proposal from the Director General of the Agence nationale de sécurité du médicament et des produits de santé and after consultation with the Commissio…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé provides all relevant information to the European Medicines Agency, as well as to the International Narc…
Where a medical device is not intended for use in a specific part of the body, it must be considered and classified according to the most critical use as specified. Where more than one rule applies to…
Under the conditions laid down in article L. 5143-7, the regional prefect of the group's registered office approves the animal health programmes and grants approval to the groups mentioned in article…
The animal health decision taken in application of article L. 5145-2-1 or article L. 5145-2-2 is published on the website of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environn…
All in vitro diagnostic medical devices imported, placed on the market or put into service must bear the CE mark. However, CE marking is not required for devices undergoing a performance evaluation or…
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