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Showing 221–230 of 32465 articles for “Art. R 134-16”
The marketing authorisation holder may, by written reasoned request, refer the matter to the Committee for Medicinal Products for Human Use referred to in Article 56 of Regulation (EC) No 726/2004 of…
Any company or organisation exploiting a medicinal product or a product mentioned in Article R. 5121-150 implements procedures to obtain accurate and verifiable information for the scientific evaluati…
The decision to approve or refuse approval is notified to the organisation by the prefect.
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 three months of the date on which the application…
The substitution referred to in articles R. 3221-13 and R. 3221-16 is recorded by the Prefect or the President of the Departmental Council and notified to their co-contractors.
Registration of the company in the Trade and Companies Register is governed by articles R. 123-31 et seq, subject to the provisions below. A copy of the declaration mentioned in article R. 814-160 is…
The request for re-examination relating to elements covered by Part II of the requests for substantial changes provided for in Article 20 of the aforementioned European Regulation of 16 April 2014 sha…
The chapter "Dotation départementale d'équipement des collèges" created by article L. 3334-16 is included in the budget of the Ministry of the Interior.
I. - Are applicable in the Wallis and Futuna Islands, subject to the adaptations mentioned in II, the provisions of the articles mentioned in the left-hand column of the table below, in the wording in…
The national database mentioned in article L. 1121-16 is managed by the Minister for Health and is supplied by the investigators of the research mentioned in 1° of article L. 1121-1. Its implementatio…
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