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Showing 41–50 of 51 articles for “Art. 726”
…to the Pharmacovigilance Risk Assessment Committee referred to in Article 56 of Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004. The draft protocol is submi…
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…007 on advanced therapy medicinal products and amending Directive 2001/83/EC and Regulation (EC) No 726/2004 and clinical trials of advanced therapy medicinal products as defined in 17° of Article L.…
…medicinal products which have been granted a marketing authorisation pursuant to Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004, the Agence nationale de séc…
…on value;According to the following scale: Base brackets Rate applicable 0 to €1,725 1.488% From €1,726 to €4,600 0.496% From €4,601 to €34,500 0.248% More than €34,501 0.099%The fee mentioned in the…
…sions of Chapter I of Title II of this Book or by the European Union pursuant to Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Community proced…
…007 on advanced therapy medicinal products and amending Directive 2001/83/EC and Regulation (EC) No 726/2004, and reconstitution of investigational advanced therapy medicinal products; 5° Putting into…
…is of article 80 bis of the General Tax Code, as well as from the second paragraph of II of article 726 of the same code may not be included in the plan. Units in venture capital mutual funds, shares…
…o the Committee for Pharmacovigilance Risk Assessment mentioned in Article 56 of Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004.In collaboration with the Eu…
…007 on advanced therapy medicinal products and amending Directive 2001/83/EC and Regulation (EC) No 726/2004, manufactured in France in accordance with specific quality standards and used in a hospita…
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