Article 211-97
The award of selective financial aid for the production and preparation of feature-length cinematographic works is subject to the provisions of Commission Regulation (EU) No 651/2014 of 17 June 2014 d…
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Showing 5031–5040 of 66875 articles for “Art. I-1-3°”
The award of selective financial aid for the production and preparation of feature-length cinematographic works is subject to the provisions of Commission Regulation (EU) No 651/2014 of 17 June 2014 d…
A director providing evidence of at least four years' professional practice in the speciality applied for, attested by a knowledge control examination, may have the mention of that speciality entered…
I.-The panel for the examination referred to in article R. 811-28-5 is composed as follows: 1° A professor of higher education or lecturer responsible for teaching law in the field of the speciality a…
The examination mentioned in Article R. 811-28-5 is open to judicial administrators registered on the national list mentioned in Article L. 811-2. It is organised by the Conseil national des administr…
The certificate drawn up by the person responsible for the transfer of the second-hand medical device certifies that it has undergone regular maintenance in accordance with the provisions of article R…
For the application of II of Article L. 561-32, the persons mentioned in Article L. 561-2 shall put in place an internal control system adapted to their size, the nature, complexity and volume of thei…
The marketing authorisation holder shall forward without delay to the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail, including duri…
For the purposes of Article L. 5141-5, type II variations and extensions as defined in 3° and 4° of Article 2 of Commission Regulation (EC) No 1234/2008 of 28 November 2008 concerning the examination…
In the event of a change in the classification or maximum residue limit of a pharmacologically active substance in application of Regulation (EC) No 470/2009 of the European Parliament and of the Coun…
Where a medicinal product has obtained an initial marketing authorisation in accordance with Article L. 5141-5, any variation or extension, as provided for in Chapter I of Commission Regulation (EC) N…
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