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Showing 1481–1490 of 37960 articles for “Art. L 227-16”
The decision of the Director General of the Autorité des relations sociales des plateformes d'emploi mentioned in article R. 7343-14 may be contested by the elector or by a representative appointed by…
The establishment is subject to the provisions of Titles I and III of Decree no. 2012-1246 of 7 November 2012 on public budgetary and accounting management.
The results of the analyses and the conclusions of the analysis report are communicated to the officials who drew up the report or the sampling record and, as appropriate, to the Agence nationale de s…
The provisions of 1° of article R. 5132-15 do not apply to the medicinal products mentioned in 2° and 3° of article R. 5124-43. However, the words: "Reserved for professional use", surrounded by a col…
The authorisation holder shall inform the Director General of the Agency of the commencement of the activity covered by the authorisation. He shall also inform him of the definitive cessation of this…
The application for marketing authorisation is accompanied by a dossier containing : 1° The administrative information required to examine the application ; 2° Scientific documentation demonstrating t…
In the companies and their establishments mentioned in 1° and 2° of article R. 5142-1, the pharmacist or veterinarian in charge and the delegated pharmacist(s) or veterinarian(s) must have at least tw…
The CE mark is affixed under the responsibility of the manufacturer or his authorised representative. Its form and dimensions are laid down by order of the Minister for Health. The CE marking must be…
In order to comply with the requirements relating to design and manufacture, in vitro diagnostic medical devices are designed, manufactured and packaged in such a way as to meet the following objectiv…
The reports, whether mandatory or optional, provided for in articles R. 5212-14 and R. 5212-15 are made by manufacturers or their representatives, users or third parties who observe or are aware of in…
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