Article 627-19
Upon arrival in France, the transferred person is presented to the public prosecutor of the place of arrival, who will question the person and draw up a report. However, if the examination cannot be c…
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Showing 2431–2440 of 22664 articles for “Art. Cass. crim. 30 janvier 2019 n° 17-85304”
Upon arrival in France, the transferred person is presented to the public prosecutor of the place of arrival, who will question the person and draw up a report. However, if the examination cannot be c…
If the sentenced person applies for work release, semi-liberty, reduction of sentence, splitting or suspension of sentence, home detention under electronic monitoring or conditional release, the appli…
The rights of access and rectification provided for in articles 39 et 40 de la loi n° 78-17 du 6 janvier 1978 relative à l'informatique, aux fichiers et aux libertés s'exercent auprès de la direction…
The application for authorisation is deemed to be complete if, within one month of receipt, the Director General of the Agence nationale de sécurité du médicament et des produits de santé has not info…
For the purposes of this section, advanced therapy medicinal products prepared on an ad hoc basis mean the advanced therapy medicinal products mentioned in 17° of Article L. 5121-1.For the purposes of…
The Agence de la biomédecine is informed of the decisions taken in application of Article R. 5121-212.
The authorisation may be subject to special conditions requiring the beneficiary of the authorisation to implement a plan for monitoring the efficacy and safety of the medicinal product, including the…
I. - The application for authorisation of an individually prepared advanced therapy medicinal product is accompanied by a dossier, the content of which is laid down by decision of the Director General…
In the event of failure to comply with the legislative and regulatory requirements, the conditions for granting or monitoring the authorisation referred to in Articles R. 5121-212 and R. 5121-213, or…
A request for authorisation must be submitted for any changes which have an impact on the quality, safety and efficacy of the medicinal product. This application must be accompanied by a technical dos…
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