Article R5146-2
…a report drawn up as part of an inspection as referred to in Article 80 of Directive 2001/82/EC of 6 November 2001 on the Community code relating to veterinary medicinal products for the purpose of m…
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Showing 10821–10830 of 39241 articles for “Art. al. 6”
…a report drawn up as part of an inspection as referred to in Article 80 of Directive 2001/82/EC of 6 November 2001 on the Community code relating to veterinary medicinal products for the purpose of m…
…ité sanitaire de l'alimentation, de l'environnement et du travail mentioned in 1° of Articles L. 5146-1 and L. 5146-2 and to the official veterinarians mentioned in 3° of the same Articles.
As part of the EC declaration of conformity procedure, production quality assurance, for active implantable medical devices or medical devices in class IIb or class III, the manufacturer submits an ap…
The medical devices which must be notified in accordance with Article L. 5211-4 are class IIa, IIb and III medical devices and active implantable medical devices. The communication is made to the Dire…
When advertising in favour of a veterinary pharmaceutical company or establishment mentions a veterinary medicinal product, it is governed by the provisions of Section 8 of Chapter I of this Title. Th…
…dies it has authorised to ensure ongoing compliance with the obligations listed in Article R. 5211-56, under the conditions laid down in Article 5 of Implementing Regulation (EU) No 920/2013.
…the inspections carried out. 5° The approved body takes out insurance covering its civil liability; 6° At the request of the Director General of the Agence nationale de sécurité du médicament et des p…
When medicated feed is supplied to a distributor or breeder in closed packaging or containers, the way in which the packaging or containers are closed prevents them from being reused after opening.
A custom-made device is any medical device manufactured specifically in accordance with the written prescription of a duly qualified practitioner, or any other person who is authorised to do so by vir…
A natural or legal person who assembles devices bearing the CE marking, in accordance with their intended purpose and within the limits of use laid down by their manufacturers, in order to place them…
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