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Showing 8501–8510 of 50062 articles for “Art. s. R 622-8 to R 622-9”
For the application of this book in French Polynesia: 1° The references to the Prefect are replaced by the reference to the High Commissioner of the Republic in French Polynesia; 2° The references to…
The decisions of the Board of Directors relating to 8°, 9°, 10°, 11°, 13° and 19° of I of article R. 6123-8 are automatically enforceable fifteen days after they are received by the ministers responsi…
The information sent, pursuant to Article L. 4311-15-1, by the bodies issuing evidence of formal qualifications to the service or body responsible for registering the persons referred to in Article L.…
The information referred to in article R. 4311-105 is transmitted when the training title is obtained or the level of training is recognised.
Establishments or organisations which store and distribute individually prepared advanced therapy medicinal products which have been transferred to them by an establishment or organisation authorised…
I. - The Director General of the Agence nationale de sécurité du médicament et des produits de santé will notify the applicant of his decision within ninety days from the date of receipt of the applic…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé will send a copy of the complete application to the Director General of the Agence de la biomédecine for…
The establishment or authorised body must send the Director General of the Agence nationale de sécurité du médicament et des produits de santé a copy of any instrument appointing the responsible perso…
Applicant establishments or organisations are required to have: 1° Premises fitted out, arranged and maintained in accordance with the rules of good practice provided for in the first or third paragra…
Applicant establishments or organisations appoint a responsible person who ensures compliance with the regulations relating to the quality and safety of advanced therapy medicinal products prepared on…
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