Article R821-14-1
The staff of the departments of the High Council is composed in accordance with Article 16 of Law No. 2017-55 of 20 January 2017 on the general statute of independent administrative authorities and in…
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Showing 1381–1390 of 4213 articles for “Art. CE 31 Mar 2017 n° 401059”
The staff of the departments of the High Council is composed in accordance with Article 16 of Law No. 2017-55 of 20 January 2017 on the general statute of independent administrative authorities and in…
Commission Delegated Regulation (EU) 2017/591 of 1 December 2016 clarifies the definition of economically equivalent OTC contracts.
…ject to the adaptations provided for in this chapter, the following provisions shall apply to Saint-Martin in their wording resulting from Ordinance No. 2020-1733 of 16 December 2020, unless otherwise…
…the following provisions are applicable to Saint-Barthélemy in their wording resulting from Ordinance No. 2020-1733 of 16 December 2020, unless otherwise stated in the table below.Articles applicable…
…nue generated as from this date, the revenue generated between 22 June 2020 and 1 September 2020. Receipts made before 14 March 2020 are not taken into account when determining these rates, except in…
…ht-hand column of the same table:Applicable articlesIn the wording resulting from the decreeD. 526-2n° 2013-372 of 2 May 2013D. 526-3No. 2019-191 of 14 March 2019D. 526-5n° 2019-191 of 14 March 2019
…ht-hand column of the same table:Applicable articlesIn the wording resulting from the decreeD. 526-2n° 2013-372 of 2 May 2013D. 526-3No. 2019-191 of 14 March 2019D. 526-5n° 2019-191 of 14 March 2019
When a medicinal product is the subject of a marketing authorisation granted by the European Union pursuant to Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 200…
In order to obtain a marketing authorisation for a medicinal product which is not covered by the marketing authorisation procedure issued by the European Commission pursuant to Regulation (EC) No 726/…
I.-If the manufacturer of a device referred to in Article 1 of Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 or, where applicable, its authorised representativ…
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