Article R5132-74
The production, including cultivation, manufacture, transport, import, export, possession, offering, transfer, acquisition or use and, in general, agricultural, craft, commercial and industrial operat…
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Showing 4311–4320 of 18903 articles for “Art. D 815-7”
The production, including cultivation, manufacture, transport, import, export, possession, offering, transfer, acquisition or use and, in general, agricultural, craft, commercial and industrial operat…
Doctors, veterinary surgeons and the groups defined in article L. 5143-6 who are authorised to supply medicinal products are subject to the obligations imposed on pharmacists by this chapter, subject,…
The authorisation provided for in Article R. 5132-74 is issued by the Director General of the Agence nationale de sécurité du médicament et des produits de santé, after obtaining the opinion of the Di…
Containers or packaging containing narcotics and used for their import or export, transport or possession must bear a label of a size appropriate to their volume, affixed in such a way that it cannot…
Active substances may only be imported for the manufacture of medicinal products for human use from a third country into the European Union if they are accompanied by written confirmation from the com…
When the application for authorisation concerns all or part of the micro-organisms or toxins or products containing them, intended for veterinary use, the Director General of the Agence nationale de s…
The registration of a homeopathic veterinary medicinal product mentioned in Article L. 5141-9 may be refused, suspended or withdrawn by the Director General of the Agency. Decisions to refuse, suspend…
Decisions to register homeopathic veterinary medicinal products or to suspend or cancel these registrations are made public in an extract on the website of the Agence nationale de sécurité sanitaire d…
Medicinal products subject to clinical trials, on the one hand, and any reference medicinal products and placebos, on the other, are prepared in accordance with good manufacturing practice, defined in…
In the case of small immediate packaging other than ampoules containing only one dose of use and on which it is impossible to include all the information provided for in Article R. 5141-74, the inform…
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