Article R5126-51
Under the conditions laid down in their articles of association, pharmacists belonging to one of the categories of practitioners mentioned in 1° of article L. 6152-1 may manage an internal-use pharmac…
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Showing 9331–9340 of 26790 articles for “Art. CE 5-6-2020 n° 423066”
Under the conditions laid down in their articles of association, pharmacists belonging to one of the categories of practitioners mentioned in 1° of article L. 6152-1 may manage an internal-use pharmac…
…of the European Parliament and of the Council of 30 November 2009 on cosmetic products is easily accessible to the public by appropriate means. It shall send this information by any means giving a da…
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…
…ticles L. 1421-1 to L. 1421-3, article L. 5127-2 or article L. 5313-3, a report ; - as part of a procedure to investigate and establish criminal offences under the conditions set out in article L. 541…
…technical specifications laid down, after obtaining the opinion of the Director General of the Agence nationale de sécurité du médicament et des produits de santé, by order of the Minister for Health…
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…
…ere 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 sécurit…
…ackaging and relabelling carried out in the context of the distribution of a raw material for pharmaceutical use does not comply with the good practices provided for in Article L. 5138-3, the inspecte…
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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