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Showing 5251–5260 of 49555 articles for “Art. L. 125-5 V + jurisprudence”
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…
…se of medicinal products or products intended for human medicine or medicinal products intended for veterinary medicine, classified as narcotics or subject to narcotics regulations, are written on a p…
…cle R. 5132-58, whether free of charge or in return for payment, is recorded using a procedure approved by order of the ministers responsible for agriculture, consumer affairs, industry and health, wh…
…santé shall notify the manufacturer, importer or distributor, informing it of his intentions and inviting it to submit its observations within a period which may not exceed one month. In the light of…
…plete, the Director General of the Agency will set the deadline by which these documents must be provided.
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…
…sponsible 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 sécurité sanitaire de l'alimentation, de…
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…
…nting at the request of the control authorities and not allowing any modification of the data after validation of their recording. The registers, records and paper copies of these records for periods…
…rticle R. 5142-55 ensures that the medicated feedingstuffs manufactured in this way are used exclusively within the framework of the clinical trial carried out under the conditions provided for in art…
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