Article R5132-5
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…
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Showing 6041–6050 of 31508 articles for “Art. Cass. 3e Civ. 19-5-1999 n° 97-18.057”
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…
The conditions under which emergency contraception not subject to compulsory prescription may be administered to day and boarding pupils in secondary education establishments, in application of the pr…
When the inspection reveals that the manufacture or repackaging and relabelling carried out in the context of the distribution of a raw material for pharmaceutical use does not comply with the good pr…
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…
The marketing authorisation holder responsible for the study referred to in Article R. 5141-30 shall make the study protocol and report available to the Director General of the Agence nationale de séc…
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…
The depositories defined in 4° of article R. 5142-1 carry out their activities under the conditions set out in a written contract which, in accordance with the good practices provided for in article L…
When medicated feedingstuffs are manufactured for the purposes of a clinical trial, they are manufactured in accordance with the sponsor's instructions. The person responsible referred to in article R…
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