Article R2121-6
In the event of the provisional suspension of the town council provided for in the second paragraph of article L. 2121-6, the prefect shall immediately report to the Minister of the Interior.
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Showing 6351–6360 of 56936 articles for “Art. I-3°”
In the event of the provisional suspension of the town council provided for in the second paragraph of article L. 2121-6, the prefect shall immediately report to the Minister of the Interior.
The Director General of the Agence nationale de sécurité du médicament et des produits de santé may, by a reasoned decision setting out the appeal procedures and deadlines, automatically vary, suspend…
The specific obligations which may be imposed pursuant to the third paragraph of Article L. 5121-9 and which must be mentioned in the risk management system are, in particular, the following: 1° The a…
The marketing authorisation is renewable on application by the holder to the National Agency for the Safety of Medicines and Health Products no later than nine months before its expiry date. The appli…
In the case of blood-derived medicinal products, the Agence nationale de sécurité du médicament et des produits de santé may, when examining the application for marketing authorisation, submit samples…
When, on the occasion of the implementation of Article 20(4) of Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004, urgent action is essential to protect human…
The Director General of the Agence de sécurité du médicament et des produits de santé (Agency for the Safety of Medicines and Health Products) makes public, in particular via the Agency's website: 1°…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé may prohibit the prescription and supply of a proprietary medicinal product and withdraw it from the mar…
Without prejudice to the provisions of 2° of Article R. 5121-50, each year the Agence nationale de sécurité du médicament et des produits de santé publishes on its website the list of medicinal produc…
When a medicinal product has obtained an initial marketing authorisation in accordance with Article L. 5121-8, any variation or extension, as provided for in Chapter I of Commission Regulation (EC) No…
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