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Showing 521–530 of 47859 articles for “Art. 151 septies · CE plén. 13 June 2018 n° 401942 · CE 17 May 1995 · CE 26 September 2018 · CE 28 April 2006 · CAA Paris 9 November 2011 · BOI-BIC-PVMV-40-10-10-10 et -20”
…pter lays down the rules applicable, with a view to facilitating the social rehabilitation of sentenced persons, to the recognition and enforcement, in a Member State of the European Union, of final c…
The anonymity of the staff of the French Office for the Protection of Refugees and Stateless Persons responsible for examining asylum applications and conducting personal interviews with applicants is…
…n calculating their prudential technical provisions, within the meaning of Article L. 351-2, insurance and reinsurance undertakings shall take account of the value of financial guarantees and any opti…
In the establishments, services or organisations mentioned in I of Article L. 5126-10 which do not have an in-house pharmacy, the medicinal products, products or articles mentioned in Article L. 4211-…
By way of derogation from the provisions of article R. 5121-99, the registration lapses if it appears that it is not followed by the marketing of the medicinal product on the national territory within…
…ion has been granted, which could lead to a change in the registration dossier. This information concerns in particular the assessment of the quality, safety and homeopathic use of the medicinal produ…
After registration, manufacturing methods and control techniques take account of scientific and technical progress. Any resulting changes must first be registered under the conditions set out in artic…
…is suspended or withdrawn, the holder informs the stockholders without delay. They must take all necessary steps to stop the distribution of the medicinal product. If these steps are not taken within…
Registration of homeopathic medicinal products and traditional herbal medicinal products, as well as suspension and withdrawal of registration, are made available to the public by the Director General…
A medicinal product or a series of medicinal products mentioned in Article L. 5121-13 may only be registered if the applicant is established in a Member State of the European Community or a party to t…
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