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Showing 1671–1680 of 3965 articles for “Art. no. 17-31052”
A request for authorisation must be submitted for any changes which have an impact on the quality, safety and efficacy of the medicinal product. This application must be accompanied by a technical dos…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé will notify the applicant of his decision within a maximum of one hundred and twenty days from the date…
The official receiver shall authorise the judicial representative appointed in the main insolvency proceedings opened by a court located on the national territory to make, pursuant to Article 36 of th…
A decree in Council of State shall specify the conditions of application of this chapter.
Without prejudice to the remedies otherwise open to them, the public prosecutor, by way of appeal, and any creditor, by way of appeal or third party opposition, as the case may be, may challenge the d…
The court shall rule on challenges raised or applications made, in accordance with paragraphs 7 or 8 of Article 36 of the aforementioned Regulation (EU) No 2015/848, by the local creditors of an estab…
The court is seised by petition of challenges raised or applications made pursuant to Article L. 691-3. The court rules on the application after hearing or duly calling in chambers the debtor who has…
If classes of creditors have been constituted, the official receiver shall collect, by any means, their opinions on the draft undertaking mentioned in Article L. 691-2. He informs the juge-commissaire…
The provisions of sub-section 2 of section 7 of this chapter relating to cancer treatment activities are applicable to the holder of the authorisation under grades C and D when it carries out interven…
Authorisation for interventional radiology activities may be issued for the following categories : 1° Category A including, with the exception of procedures specifically covered by categories B, C and…
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