Article R8115-3
The decision of the Regional Director of Business, Competition, Consumer Affairs, Labour and Employment will indicate the appeal procedures and deadlines.
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Showing 8941–8950 of 51798 articles for “Art. L 151-3”
The decision of the Regional Director of Business, Competition, Consumer Affairs, Labour and Employment will indicate the appeal procedures and deadlines.
The pharmacist in charge of managing the internal-use pharmacy is responsible for the tasks and activities authorised for that pharmacy. The staff assigned to the pharmacy perform their duties under t…
The time spent by the pharmacist in charge of managing an in-house pharmacy in an establishment may not be less than the equivalent of five half-days per week. However, in medico-social establishments…
The content of the information provided for in articles R. 5133-1 and R. 5133-2 for reagents requiring special precautions for use may be specified, on a proposal from the Director General of the Agen…
When a minor has been dispensed the medicinal products indicated in the emergency contraception, the pharmacist sends the health insurance fund to which he belongs an invoice drawn up on a care sheet…
The natural or legal person who initiates a veterinary medicinal product trial as defined in article R. 5141-2 is called the sponsor. The persons who direct and supervise the performance of pharmaceut…
…appointment when it expires, the pharmacist or veterinary surgeon may refer the matter to the central council of the competent section of the national order of pharmacists or the regional council of t…
The companies mentioned in article R. 5142-1 may export the veterinary medicinal products they sell, transfer free of charge or distribute outside national territory.Exports by these companies to othe…
The company sends the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail a copy of any document appointing the pharmacist or veterinaria…
As part of the EC declaration of conformity procedure, the manufacturer shall draw up technical documentation making it possible to assess the conformity of the medical device with the essential requi…
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