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Showing 5511–5520 of 47938 articles for “Art. Cass. 3e civ. 15 December 2010 · Cass. 1re civ. 5 December 1995 · Cass. 3e civ. 5 December 1984 · Cass. 3e civ. 24 September 2008 · Cass. 3e civ. 30 January 2020 · Cass. 3e civ. 10 December 1986 · Cass. com. 4 June 1996 · Cass. 3e civ. 27 February 1991”
A plasma paste is any intermediate product resulting from the fractionation of plasma, whatever its level of processing, which cannot be used as it is for administration to humans, and which is intend…
This section applies to plasma pastes and labile blood products intended for the preparation of health products. It also applies to labile blood products for direct therapeutic use included on the lis…
The automated national register instituted by Article L. 1232-1 shall be operated and managed by the Agence de la biomédecine under the conditions laid down in this section.
The information contained in the promotional communication is accurate, up-to-date, verifiable and sufficiently complete to enable healthcare professionals to assess the therapeutic value of the produ…
…t apply to the Armed Forces Blood Transfusion Centre, subject to the provisions of articles R. 1222-47, R. 1222-50 and R. 1222-51.
…t of the Etablissement Français du Sang in accordance with the procedure set out in Article R. 1222-50. However, the opinion of the Regional Health Agency is not required for amendments to the plans r…
The committee of experts set up by the Agence de la biomédecine under the conditions set out in article L. 1231-3 sits on one of the sites designated by the latter. The list of sites is communicated t…
Where the activities referred to in article R. 1243-49 are carried out in separate locations, the organisation may submit several declarations, determining the scope covered by each of them.
A copy of the complete dossier is sent by the Director General of the Agence nationale de sécurité du médicament et des produits de santé to the Director General of the Agence de la biomédecine. The D…
Five copies of the application for authorisation or renewal of the authorisation must be sent by registered post with acknowledgement of receipt to the Director General of the Regional Health Agency.…
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