Article R5126-51
…nder 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 pharmacy…
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Showing 5791–5800 of 21091 articles for “Art. CA Paris 20-5-2009 n° 08-2432”
…nder 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 pharmacy…
Where the internal-use pharmacy of a health care institution is authorised to supply medicinal products or health care products to the public pursuant to 1° and 2° of Article L. 5126-6 or Article L. 6…
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…
A sample shall give rise, on the spot, to the drafting of : - as part of an inspection carried out under the conditions laid down in articles L. 1421-1 to L. 1421-3, article L. 5127-2 or article L. 53…
…s narcotics or subject to narcotics regulations, are written on a prescription that meets the technical specifications laid down, after obtaining the opinion of the Director General of the Agence nati…
…umer affairs, industry and health, which allows the competent authorities to monitor the operations carried out. These records indicate the name and quantity of the substances or preparations transfer…
…t subject to compulsory prescription may be administered to day and boarding pupils in secondary education establishments, in application of the provisions of the second paragraph of I of article L. 5…
…he rules laid down in this chapter, the Director General of the Agence nationale de sécurité du médicament et des produits de santé shall notify the manufacturer, importer or distributor, informing it…
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…
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