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Showing 6271–6280 of 67437 articles for “Art. I-5° bis and Art. 35 bis”
The procedures for issuing communication permits to lawyers and the rules applicable to relations between detainees and their defence counsel are determined by the provisions of articles R. 313-14, R.…
…ing division in order to examine the progress of proceedings with a view to ensuring the efficiency and speed of the information for which its members are responsible. These meetings may only concern…
…eneral of the regional health agency.A copy of this decision is sent to the regional haemovigilance and transfusion safety coordinator and to the Etablissement Français du Sang or, where applicable, t…
…Papeete Papeete Paris Paris Bayonne Pau La Rochelle Poitiers Troyes Reims Brest Rennes Clermont-Ferrand Riom Rouen Rouen Saint-Pierre Saint-Denis de La Réunion Saint-Pierre-et-Miquelon Saint-Pierre-et…
…ent by the Agence nationale de sécurité du médicament et des produits de santé of a therapeutic use and patient monitoring protocol. This protocol specifies in particular the indication concerned, the…
…cts of major therapeutic interest referred to in article L. 5111-4, marketing authorisation holders and pharmaceutical companies exploiting medicinal products shall, under their responsibility, draw u…
…ther Member State of the European Community or party to the Agreement on the European Economic Area and are manufactured or imported in accordance with the requirements of Directive 2003/94/EC and by…
…t which manufactures medicinal products shall check that the medicinal product concerned is genuine and has not been tampered with.
…he provisions of the first sub-section, the provisions of this sub-section apply to the manufacture and importation of investigational medicinal products.
…importing investigational medicinal products under the conditions set out in articles R. 5124-57-3 and R. 5124-57-4 hold these documents and keep them for the same period of time. When the trials lea…
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