Article L5124-17-1
…s, a decision by the Director General of the regional health agency with territorial jurisdiction governs the organisation of the said system. The procedures for organising the on-call system are dete…
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Showing 4491–4500 of 36520 articles for “Art. IV & V”
…s, a decision by the Director General of the regional health agency with territorial jurisdiction governs the organisation of the said system. The procedures for organising the on-call system are dete…
In the case of research involving the human person relating to the gene therapy and xenogenic cell therapy preparations mentioned in 12° and 13° of Article L. 5121-1, the authorisation to conduct the…
In the absence of an available or suitable pharmaceutical speciality, the medical supply establishments of the armed forces health service may, in order to meet specific defence requirements, import,…
Wholesaler-distributors are required to comply with the public service obligations determined by decree in the Conseil d'Etat within their distribution territory.They ensure continuous supply to the n…
…tioned in II and III of article L. 5124-8 are manufactured in accordance with the good practices provided for in article L. 5138-3, subject to adaptations made necessary by specific defence requiremen…
Notwithstanding the provisions of Article L. 4211-1 and those of the first paragraph of Article L. 5124-2, Institut Pasteur remains authorised to ensure, in accordance with its statutes, the preparati…
…rançais du fractionnement et des biotechnologies" carries out research, production and marketing activities for medicinal products for human use, in particular medicinal products derived from blood, m…
Pharmaceutical companies and establishments may only be advertised in accordance with the conditions laid down by regulation.
When the wholesaler-distributor has fulfilled its public service obligations as set out in article L. 5124-17-2, it may sell medicinal products outside the national territory or to wholesale distribut…
…and of the Council of 31 March 2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agen…
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