Article L1123-7-2
When the National Agency for the Safety of Medicines and Health Products, the High Authority for Health, the Minister for Health or the European Medicines Agency refers a non-interventional research p…
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Showing 8981–8990 of 59535 articles for “Art. L 132-5-2”
When the National Agency for the Safety of Medicines and Health Products, the High Authority for Health, the Minister for Health or the European Medicines Agency refers a non-interventional research p…
Applications for a declaration that there are no grounds for refusing recognition and for refusal of recognition respectively made pursuant to Articles 30 and 40 of Council Regulation (EU) 2019/1111 o…
French undertakings subject to State control under article L. 310-1 and constituted in the form of a société anonyme must have share capital, excluding contributions in kind, of at least 800,000 euros…
When the foreign national applying for a multi-annual residence permit bearing the words "mobile ICT employee (family)" as provided for in article L. 421-28 resides outside France, the decision to iss…
For its application in New Caledonia, article L. 123-11-6 is worded as follows: Art. L. 123-11-6 -Customs officers are qualified to investigate and establish breaches of the provisions of this sub-sec…
Article L. 533-22-1 of the Monetary and Financial Code applies to supplementary occupational pension funds.
For the purposes of investigating market abuse as defined by Regulation (EU) No 596/2014 of the European Parliament and of the Council of 16 April 2014 on market abuse (Market Abuse Regulation) and re…
When a syndicat de communes already exercises, on behalf of the communes that make it up, the competencies set by the present code for communities of agglomerations or communities of communes, this sy…
Declarations made by insurance undertakings to the guarantee fund indicating the items to be taken into account for the assessment of the contributions referred to in articles L. 421-10 and L. 421-10-…
Inclusion on the list defined in article L. 1121-15 of clinical trials prior to the granting of marketing authorisation is compulsory.
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