Article R5134-171
In each education authority concerned, a committee chaired by the education authority rector or his representative checks whether applicants for a teaching post of the future meet the conditions enabl…
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Showing 3451–3460 of 9202 articles for “Art. Commission européenne M.5449”
In each education authority concerned, a committee chaired by the education authority rector or his representative checks whether applicants for a teaching post of the future meet the conditions enabl…
Without prejudice to the provisions of article R. 6152-413, a contractual practitioner who has an open-ended contract as provided for in article R. 6152-403 may be dismissed, after receiving the opini…
I. - The money market instruments referred to in 5° of I of article R. 214-11 are :1° Issued or guaranteed by :a) A Member State of the European Union or another State party to the Agreement on the Eu…
I. - Nationals of France or of another Member State of the European Union or of a State party to the Agreement on the European Economic Area may obtain the professional guide-lecturer card referred to…
I.-The undertakings referred to in the first paragraph of Article R. 356-8 may apply on behalf of the group and the related undertakings concerned to the Autorité de contrôle prudentiel et de résoluti…
I.-The declaration provided for in Article 3 of Regulation (EU) 2018/1672 of the European Parliament and of the Council of 23 October 2018 on controls of cash entering or leaving the Union and the dec…
…9, Article 10, paragraphs 1 to 3 of Article 11, paragraph 6 of Article 16 and Article 20 of amended Commission Regulation (EC) No 543/2008 of 16 June 2008 laying down detailed rules for implementing C…
I. - Where the applicant does not meet the requirements referred to in article L. 2223-48, he must justify: 1° If the application for recognition relates to the activity of thanatopraxy: a) A diploma,…
I.-Where the Autorité de contrôle prudentiel et de résolution is informed by the group supervisor, in the case of a supervisory authority of another Member State, of a request for authorisation to cal…
A company operating a veterinary medicinal product must: 1° Keep detailed records of all suspected adverse reactions which have occurred inside or outside the European Union; 2° To record any suspecte…
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