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Showing 311–320 of 30622 articles for “Art. R 581-36”
The marketing authorisation issued by the Agence nationale de sécurité du médicament et des produits de santé lapses if it transpires that: 1° That it is not followed by the marketing of the medicinal…
The marketing authorisation may impose one or more of the following conditions, which must be mentioned in the risk management system: 1° The implementation of measures to ensure the safe use of the m…
Implantable medical devices, active implantable medical devices and class III devices must be subject to clinical investigations, unless the use of existing clinical data can be duly justified.
I. - Authorisation for 1° under the adult critical care modality and for 1° and 2° under the paediatric critical care modality may only be granted if the holder has access, on site or by agreement, to…
I-Subject to the provisions mentioned in II and III, the articles mentioned in the left-hand column of the table below shall apply in the Wallis and Futuna Islands in the wording indicated in the righ…
For the purposes of assessing the threshold referred to in Article D. 2315-35, annual resources are equal to the total of: 1° The amount of the operating grant provided for in Article L. 2315-61 ; 2°…
The correlation tables referred to in Article R. 6123-34 are updated and distributed no later than two months after the monthly declaration of companies.
The Chairman sets the agenda for the meetings. The Chairman informs the Director General for Health, who may request that new items be added to the agenda. Opinions are adopted by a simple majority of…
I. - Supervision of compliance by the persons referred to in Article L. 561-2 with the obligations laid down in Chapters I and II of this Title, with directly applicable European provisions relating t…
The diplôme d'Etat de la jeunesse, de l'éducation populaire et du sport (state diploma in youth, popular education and sport) is awarded for the speciality of "sports development" or for the specialit…
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