Article R7227-18
…an employee must, when he wishes to benefit from the training leave referred to in article L. 7227-13, submit his request in writing to his employer at least thirty days in advance, specifying the da…
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Showing 3921–3930 of 5749 articles for “Art. 13 April 1983”
…an employee must, when he wishes to benefit from the training leave referred to in article L. 7227-13, submit his request in writing to his employer at least thirty days in advance, specifying the da…
…ommittee. It guides and monitors the work of the planned commissions mentioned in article R. 6123-3-13.It is responsible for consultation between the State, the region and the professional organisatio…
…36 of 30 August 2023L. 612-2 with the exception of 7° and 12° of A, B of I and IIILaw 2021-402 of 8 April 2021 L. 612-3 Law no. 2022-1726 of 30 December 2022L. 612-4 Order no. 2017-1608 of 27 November…
…36 of 30 August 2023L. 612-2 with the exception of 7° and 12° of A, B of I and IIILaw 2021-402 of 8 April 2021 L. 612-3 Law no. 2022-1726 of 30 December 2022L. 612-4 Order no. 2017-1608 of 27 November…
…tions laid down by the rules in force in mainland France pursuant to Regulation (EU) 2016/679 of 27 April 2016 and by Act no. 78-17 of 6 January 1978 relating to information technology, files and free…
…L. 133-1 and…
…Article 3(1)(9) of Regulation (EU) No 596/2014 of the European Parliament and of the Council of 16 April 2014 on market abuse (Market Abuse Regulation) and repealing Directive 2003/6/EC of the Europe…
…8 of Article 11 of Regulation (EU) No 596/2014 of the European Parliament and of the Council of 16 April 2014 on market abuse (Market Abuse Regulation) and repealing Directive 2003/6/EC of the Europe…
…thin the meaning of Regulation (EC) No 882/2004 of the European Parliament and of the Council of 29 April 2004 as amended on official controls performed to ensure the verification of compliance with f…
…ope of Article 1 of Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use and repealing Directive 2001/20/ E…
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