Article R8122-5
The number of sub-departmental, departmental or inter-departmental inspection units and their location are set for each region by order of the Minister responsible for labour. When sectoral or themati…
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Showing 4741–4750 of 43273 articles for “Art. Cass. com. 5 May 2004”
The number of sub-departmental, departmental or inter-departmental inspection units and their location are set for each region by order of the Minister responsible for labour. When sectoral or themati…
The list mentioned in 1° of article L. 5126-6, medicinal products : 1° Registered on the initiative of the Director General of the Agence nationale de sécurité du médicament et des produits de santé,…
The pharmacist responsible for managing the in-house pharmacy is appointed by the legal representative of the legal entity concerned.
…ernal use pharmacies of the establishments, services or organisations mentioned in 1° of article R. 5126-1, with the exception of the Institution nationale des invalides. For the purposes of this sect…
…supply medicinal products or health care products to the public pursuant to 1° and 2° of Article L. 5126-6 or Article L. 6111-1-1, the internal-use pharmacy premises must be equipped in such a way as…
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…
…nspection carried out under the conditions laid down in articles 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 crimin…
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…
…material for pharmaceutical use does not comply with the good practices provided for in Article L. 5138-3, the inspected establishment shall immediately inform the manufacturers of the medicinal prod…
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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