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Showing 5081–5090 of 43903 articles for “Art. L 227-5”
The time limit for complying with formal notices and the time limits for appeals run from the day of delivery of the notice or the day of presentation of the registered letter.
The number of sub-departmental, departmental or inter-departmental inspection units and their location are set for each region by order of the Minister responsible for labour. When sectoral or themati…
The pharmacist responsible for managing the in-house pharmacy is appointed by the legal representative of the legal entity concerned.
The provisions of this section apply to the internal use pharmacies of the establishments, services or organisations mentioned in 1° of article R. 5126-1, with the exception of the Institution nationa…
The responsible person shall ensure that the information referred to in Article 21 of Regulation (EC) No 1223/2009 of the European Parliament and of the Council of 30 November 2009 on cosmetic product…
Dangerous substances or preparations classified as very toxic, toxic, carcinogenic, teratogenic or mutagenic may only be transferred, whether free of charge or for consideration, to a natural or legal…
Prescriptions and all orders for professional use of medicinal products or products intended for human medicine or medicinal products intended for veterinary medicine, classified as narcotics or subje…
The transfer of the substances or preparations referred to in article R. 5132-58, whether free of charge or in return for payment, is recorded using a procedure approved by order of the ministers resp…
Where it appears that a reagent presents risks to public health, including as a result of non-compliance with the rules laid down in this chapter, the Director General of the Agence nationale de sécur…
The application for authorisation is deemed to be complete if, within 30 days of receipt, the Director General of the Agence nationale de sécurité du médicament et des produits de santé has not inform…
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