Article R5141-121
The registers or records mentioned in articles R. 5141-118 to R. 5141-120 are kept for five years and must be produced whenever required by the competent authorities. The recording systems comply with…
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Showing 1901–1910 of 5857 articles for “Art. 12 juill. 2018”
The registers or records mentioned in articles R. 5141-118 to R. 5141-120 are kept for five years and must be produced whenever required by the competent authorities. The recording systems comply with…
…t du travail. This authorisation is granted either under the conditions set out in articles R. 5141-123-2 to R. 5141-123-5, or under the parallel import authorisation defined in articles R. 5141-123-6…
…for human use classified in one of the categories subject to restricted prescription by article R. 5121-77, benefiting from a marketing authorisation, necessary to avoid unacceptable suffering for the…
A veterinary surgeon who prescribes medicinal products containing substances having an oestrogenic, androgenic or gestagenic action for farm animals shall record the following information in chronolog…
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,…
The certificate accompanying medicated feedingstuffs manufactured in another Member State of the European Union or party to the Agreement on the European Economic Area when they are imported correspon…
Veterinarians providing the services referred to in Article L. 5141-15 who comply with the provisions of Article L. 241-3 of the Rural and Maritime Fishing Code may use in France veterinary medicinal…
The Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail, at the request of a veterinary pharmaceutical establishment exporting a veterina…
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…
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