Article R5127-13
When, because of the quality or quantity of a product, it is impossible to divide it into three samples, the official taking the sample shall seal the entire product in a single sample.
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Showing 1791–1800 of 23443 articles for “Art. Cass. 1re civ. 13 April 1999 · Cass. 1re civ. 13 July 2004 · Cass. 3e civ. 24 June 1971”
When, because of the quality or quantity of a product, it is impossible to divide it into three samples, the official taking the sample shall seal the entire product in a single sample.
The Direction Générale de la Consommation, de la Concurrence et de la Répression des Fraudes communicates to the Agence Nationale de Sécurité du Médicament et des Produits de Santé the declarations of…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé keeps an up-to-date list of authorisation holders and authorised persons. These lists are accessible at…
Advertising to the public for a product or object defined in article R. 5134-11 may not include any element which : 1° Suggest that the effect of the product or object is guaranteed or that it has no…
Any modification concerning the elements and documents mentioned in Article R. 5141-130 is submitted for authorisation to the Director General of the Agence nationale de sécurité sanitaire de l'alimen…
Decisions to authorise, modify, renew, suspend or withdraw authorisation for the preparation of autovaccines are made public in an extract on the website of the Agence nationale de sécurité sanitaire…
The authorisation holder shall inform the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail of the date on which the activity of prepar…
…niques mentioned in a, c and d of the technical dossier provided for in 3° of II of Article R. 5141-130 are modified in line with scientific and technical progress.
The Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail will notify the applicant of his decision within one hundred and twenty days from…
The presentation, at scientific or technical meetings, exhibitions or demonstrations, of medical devices which do not comply with the provisions of this Title is authorised provided that a visible sig…
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