Article R5141-123-11
…ealth within sixty days from the date of receipt of the complete application referred to in Article R. 5141-123-9 . The period mentioned in the previous paragraph is reduced to thirty days for applica…
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Showing 641–650 of 30488 articles for “Art. R. 123-168”
…ealth within sixty days from the date of receipt of the complete application referred to in Article R. 5141-123-9 . The period mentioned in the previous paragraph is reduced to thirty days for applica…
Practical training in conservation care is provided by thanatopractitioners qualified under the conditions defined in article L. 2223-45 and working in a public authority, company, association or esta…
…thorisation is issued for a period of five years. It specifies the differences mentioned in article R. 5141-123-8 with the speciality that has obtained marketing authorisation in France. An extract of…
By way of derogation from article R. 5141-123, the importation of veterinary medicinal products intended exclusively for animals whose flesh or products are not intended for human consumption is not s…
…riod of forty-five days from the date of receipt of the complete application referred to in Article R. 5141-123-3. The period mentioned in the previous paragraph is reduced to twenty days if the appli…
…roduct which has obtained marketing authorisation in France, its name within the meaning of Article R. 5141-1, and the number of this authorisation; 3° With regard to the veterinary medicinal product…
…eleased in accordance with Article 55 of the same Directive;3° Subject to the provisions of Article R. 5141-123-8, the content by weight, by volume or by number of dosage units, the summary of product…
…tle are complied with, in particular those relating to possession and supply referred to in Article R. 5141-112, labelling referred to in Articles R. 5141-73 to R. 5141-75, and the package leaflet ref…
…ain subject to the specific provisions relating to them respectively, which are set out in articles R. 5132-78, R. 5132-27 and R. 5132-91.
…tion holder in the country of origin of any serious adverse reaction, within the meaning of Article R. 5141-92, concerning the imported proprietary medicinal product, as soon as he is aware of it.
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