Article R4211-50
…repared on an ad hoc basis in accordance with the rules of good practice provided for in Article L. 5121-5 and including a description of the responsibilities and measures to be taken. The responsible…
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Showing 1481–1490 of 51809 articles for “Art. al. 3 to 5”
…repared on an ad hoc basis in accordance with the rules of good practice provided for in Article L. 5121-5 and including a description of the responsibilities and measures to be taken. The responsible…
An authorised establishment or organisation may transfer to another authorised establishment or organisation advanced therapy medicinal products prepared on an ad hoc basis with a view to their storag…
The table below sets out the provisions of this part that give rise to the application of the prior formal notice procedure and the minimum period for compliance: PROVISIONS FOR WHICH formal notice is…
The date of the elections to the departmental and interdepartmental councils of the College of Nurses and the voting procedures are set by the National Council. Nurses who have been registered with th…
…ion or registration which are imported from another Member State of the European Community or party to the Agreement on the European Economic Area, the French authorities will recognise the control re…
…nefiting from the authorisations or registration provided for in the second paragraph of Article R. 5124-49 is subject, in France, to control of the finished product when it is imported : 1° From a St…
…ceutical establishment manufacturing medicinal products mentioned in 1° of article L. 4211-1, generators, kits or precursors mentioned in 3° of this article has a documentation system comprising speci…
When the pharmacist in charge of a manufacturer, importer or operator of medicinal products other than investigational medicinal products, generators, kits or precursors referred to in 3° of article L…
The provisions of articles R. 5124-49 to R. 5124-55 are applicable to manufacturers and importers of dressing articles or articles presented as complying with the pharmacopoeia mentioned in 2° of arti…
…e manufacturer and importer of medicinal products mentioned in 1° of article L. 4211-1, or of generators, kits or precursors mentioned in 3° of the said article, shall implement a pharmaceutical quali…
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