Article D232-20
At the first meeting following their appointment, each member of the College of the French Anti-Doping Agency takes the following oath: "I swear to fulfil my duties as a member of the College of the F…
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Showing 4211–4220 of 62395 articles for “Art. Cass. com. 6 April 1993 · Cass. com. 10 March 1998 · Cass. com. 20 September 2011 n° 10-20.664 · Cass. com. 2 May 1984 · Cass. com. 26 October 1993 · Cass. com. 19 May 1998 · Cass. com. 7 November 1989”
At the first meeting following their appointment, each member of the College of the French Anti-Doping Agency takes the following oath: "I swear to fulfil my duties as a member of the College of the F…
…hin five years of the establishment of one of the zones provided for in Article 1 of Ordinance no. 86-1113 of 15 October 1986, set up to operate a business there, are exempt from this tax on profits m…
…eriods of work experience carried out during the contract concluded in application of article L. 5132-5 may not represent more than 25% of the total duration of the contract.
A lone worker may not carry out work which : 1° Involve the manual carrying of a mass in excess of 30 kg, the manual installation or removal of equipment weighing in excess of 50 kg, or the installati…
…interruption or cessation of activity of an establishment or organisation mentioned in article L. 4211-9-1, the data relating to the traceability of advanced therapy medicinal products prepared on an…
…rranted by an emergency situation, in particular that described in Article 18 of Regulation (EU) No 1093/2010, or an adverse development that is likely to threaten market liquidity or the stability of…
…fined by the decree governing the speciality, specialisation, option or complementary certificates, may be required for access to the courses provided for in articles D. 212-24, D. 212-27, D. 212-40,…
…s of the withdrawal from the list by the Commission, the information and documents mentioned in 5°, 6° and 16° of Article R. 5121-107-4.
A generic medicinal product may not be marketed until ten years have elapsed following the initial marketing authorisation of the reference medicinal product. However, this period is extended to eleve…
…ums due to the subcontractor in accordance with the same procedures as those set out in articles R. 2191-11 and R. 2191-12.
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