Article R5142-41
…armacist or assistant veterinarian recruited in application of article R. 5142-37 is absent or replaces the pharmacist or veterinarian in charge for a period of more than one month, he is replaced.
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Showing 7851–7860 of 26972 articles for “Art. CE 16-4-2012 n° 323592”
…armacist or assistant veterinarian recruited in application of article R. 5142-37 is absent or replaces the pharmacist or veterinarian in charge for a period of more than one month, he is replaced.
…ng to veterinary medicinal products. This control is carried out by the importer's veterinary pharmaceutical establishment in a Member State or party to the Agreement on the European Economic Area or…
Veterinary pharmaceutical establishments operate in accordance with the good practices mentioned in article L. 5142-3 which are applicable to them. In particular, they have : 1° Premises fitted out, a…
The establishments referred to in article R. 5142-1 shall take all necessary measures to ensure that veterinary medicinal products are transported and delivered under conditions which guarantee their…
…manufacture and deliver comply with the characteristics to which they must conform and that the necessary controls have been carried out. Manufacturers of veterinary medicinal products which are the…
…R. 5142-1 has one or more quality control departments. This department or these departments are placed under the authority of a suitably qualified person who is hierarchically independent of the othe…
As part of the EC declaration of conformity procedure, production quality assurance, the manufacturer shall submit to an authorised body for verification the quality system which he has set up for the…
In the case of active implantable medical devices or medical devices in Class III or Class II b, the manufacturer shall take all necessary measures to ensure that the manufacturing process guarantees…
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…
As part of the EC declaration of conformity procedure, product quality assurance, the manufacturer shall submit to an authorised body for verification the quality system which he has set up for the fi…
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