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Showing 2401–2410 of 33488 articles for “Art. 215 al. 3”
The Director General of the Agence nationale de sécurité du médicament et des produits de santé may require samples and mock-ups to be submitted when the medicinal product is marketed.
…the marketing authorisation lapses is counted from : 1° the date of publication of Decree No. 2008-435 of 6 May 2008 for marketing authorisations issued up to that date, with the exception of those fo…
…e use of the medicinal product or product; 2° The performance of post-authorisation safety studies; 3° Compliance with specific obligations regarding the recording or reporting of suspected adverse re…
…ement system as conditions of the marketing authorisation, in accordance with 1° of Article R. 5121-36-1.
…to medical availability, in any specialty facility corresponding to the patient's acute pathology; 3° Or in the emergency department when the patient's state of health so requires. When care is provi…
…for cancer treatment by complex oncology surgery with grade B as referred to in II of Article R. 6123-87-1 may only be granted if the applicant has an organisation enabling it to: 1° Organise the mult…
…team whose functions and tasks are defined by the operating charter provided for in article D. 6124-305 and all of whose members are trained in part-time care or outpatient anaesthesia or surgery. Thi…
The consultation provided for in Article L. 6143-7 takes place on the initiative and in accordance with the procedures defined by the Chairman of the Executive Board. In addition, the latter shall con…
…ted person is still in custody, he or she shall, except where the first subparagraph of article 695-39, released automatically.
The provisions of Article 695-37 do not preclude the Investigating Chamber, after ruling on the execution of the European arrest warrant, from temporarily postponing the surrender for serious humanita…
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