Article R1411-55-2
Each year, within the framework of the coordination body provided for in article L. 1411-5-1, the Minister for Health shall draw up a provisional list of the referrals he intends to make to the High C…
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Showing 4221–4230 of 64913 articles for “Art. R 315-5 and Art. R 315-7 s.”
Each year, within the framework of the coordination body provided for in article L. 1411-5-1, the Minister for Health shall draw up a provisional list of the referrals he intends to make to the High C…
Unless there is a risk to patients' health, proprietary medicinal products which fulfil the conditions for being a reference proprietary medicinal product in an existing generic group may, by decision…
The rules of good practice relating to: : 1° Criteria for identifying serious conditions caused by genetic abnormalities; 2° Criteria for identifying serious conditions for which there is a strong pro…
When the composition pénale includes the handing over of the vehicle for immobilisation as provided for in 3° of article 41-2, this surrender shall be carried out in accordance with the provisions of…
Except where there is a risk to patients' health, the proprietary medicinal products mentioned in b of 5° of Article L. 5121-1 which are presented in a modified-release oral pharmaceutical form differ…
I.-The applicant may apply to the Director General of Competition, Consumer Affairs and Fraud Control or the General Rapporteur of the Competition Authority for a place in the order of arrival with a…
I.-The authorities or bodies designated in III will issue a certificate to any beneficiary of the obligation to employ disabled workers mentioned in article L. 5212-2 when the decision provided for in…
I.-For the application of Article L. 111-4-1, the following sports and leisure articles are subject to the provisions of this article: 1° Bicycles, as defined in Article 1 of Decree no. 2016-364 of 29…
Audits commissioned by CCI France pursuant to 7° of Article L. 711-16 are carried out on site or on the basis of documents requested from the audited establishment and, where applicable, from the regi…
When a new indication is authorised by the Agence nationale de sécurité du médicament et des produits de santé, on the basis of preclinical and clinical studies considered significant during the scien…
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