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Showing 5201–5210 of 43956 articles for “Art. L. 145-5”
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…
The sponsor provides the investigators within the meaning of Article R. 5141-3 with the following information: 1° The title and objective of the trial requested ; 2° Identification of the medicinal pr…
…ral of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail.
Authorisation to open a veterinary pharmaceutical establishment is granted to the company to which it belongs by the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, d…
The information referred to in articles R. 5142-57 and R. 5142-58 is, immediately after each operation, recorded by an appropriate system allowing immediate printing at the request of the control auth…
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