Article R5141-122
…ne of the categories subject to restricted prescription by article R. 5121-77, benefiting from a marketing authorisation, necessary to avoid unacceptable suffering for these animals or to respond to s…
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Showing 3021–3030 of 8984 articles for “Art. n° 22-18436 · AFNOR NF K 12-500”
…ne of the categories subject to restricted prescription by article R. 5121-77, benefiting from a marketing authorisation, necessary to avoid unacceptable suffering for these animals or to respond to s…
…having an oestrogenic, androgenic or gestagenic action for farm animals shall record the following information in chronological order in a register or by any appropriate recording system: 1° Number of…
If, within a period of two years following notification of the authorisations provided for in articles R. 5142-8 to R. 5142-10, the establishment is not operating, these authorisations lapse. However,…
…which the medicated feed is intended; 4° The name, qualitative and quantitative composition and marketing authorisation number of the medicated premix used to manufacture the medicated feed; 5° The n…
…erinary medicinal products other than immunological medicinal products which have been granted a marketing authorisation in the Member State in which they practise when these medicinal products are no…
…ing practices provided for in Article L. 5142-3; 3° Where the veterinary medicinal product has a marketing authorisation, issues the summary of product characteristics or an equivalent document. Where…
The authorisation provided for in Article L. 5141-10 is issued by the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail.
Any medical device placed on the market or put into service in France must bear the CE mark certifying that it meets the conditions set out in article R. 5211-17. However, CE marking is not required f…
…in 4° of Article R. 5222-3 or in a blood transfusion establishment who are aware of incidents or risks of incidents involving an in vitro diagnostic medical device shall declare them without delay to…
Any health establishment or health cooperation group which uses or supplies medical devices or makes such devices available to its members, as well as any association distributing medical devices at h…
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