Article R7343-105
I.-The expert appoints a project manager to act as an intermediary with the Employment Platforms Social Relations Authority. The project manager must have the appropriate skills for this task. II -Whe…
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Showing 4691–4700 of 54327 articles for “Art. Cass. 1re civ. 30 October 2007 · Cass. 1re civ. 25 February 2010 · Cass. com. 3 May 2006 · Cass. com. 10 July 2012 · Cass. com. 27 January 2015”
I.-The expert appoints a project manager to act as an intermediary with the Employment Platforms Social Relations Authority. The project manager must have the appropriate skills for this task. II -Whe…
The Minister for Health shall inform the Minister for Defence, for each of the locations of the pharmacy for internal use, of the conclusions of the competent departments regarding compliance with the…
The medicinal products and products referred to in article R. 5126-108 are held in one or more premises, cupboards or other locked storage devices, or with a locking system that ensures the same secur…
…arians, pharmacists and members of the other health professions mentioned in 4° of article R. 5141-93 are subject are defined, on a proposal from the Director General of the Agence nationale de sécuri…
…an Medicines Agency in Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Community procedures for the authorisation and supervision of medicinal pr…
…for the declarations and the periodic pharmacovigilance update report mentioned in articles R. 5141-103 to R. 5141-105-1 are laid down by decision of the Director General of the Agence nationale de sé…
Where the initial authorisation was granted after the Director General of the Agence nationale de sécurité du médicament et des produits de santé or the Prefect had been informed in accordance with th…
The animal health decision taken in application of article L. 5145-2-1 or article L. 5145-2-2 is published on the website of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environn…
All in vitro diagnostic medical devices imported, placed on the market or put into service must bear the CE mark. However, CE marking is not required for devices undergoing a performance evaluation or…
…ed by the doctor responsible for medical information under the conditions laid down inarticle R. 6113-8, the representative of the establishment or, for care activities jointly operated by a health co…
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