Article R229-3
The proposed transfer to another Member State of the European Community of the registered office of a société européenne registered in France, as provided for in the first paragraph of article L. 229-…
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Showing 5551–5560 of 6290 articles for “Art. 28 March 2014”
The proposed transfer to another Member State of the European Community of the registered office of a société européenne registered in France, as provided for in the first paragraph of article L. 229-…
The Board of Directors deliberates in particular on: 1° The initial budget and any amendments to it, loans, the financial account and the allocation of the year's income; 3° The creation, sale or abol…
I. - The rules governing the composition of assets and the division of risks must be complied with at all times. However :1° General-purpose investment funds are not required to comply with the limits…
The director manages the public establishment for cultural or environmental cooperation.In this capacity:a) He draws up and implements the artistic, cultural, educational, environmental or scientific…
The Managing Director is appointed for a renewable term of three years. The age limit for the Director General is sixty-seven. He manages the agency. He performs all acts that are not reserved to the…
The constituent agreement of the National Cancer Institute is approved by order of the ministers responsible for the budget, research and health.In particular, it sets out the extent of the powers exe…
I.-The notification file referred to in Article L. 3513-10 shall contain, depending on whether it concerns an electronic vaping device or a refill bottle, the following information:1° The name and con…
In the case of blood-derived medicinal products, the Agence nationale de sécurité du médicament et des produits de santé may, when examining the application for marketing authorisation, submit samples…
For public health reasons, the Agence nationale de sécurité du médicament et des produits de santé may require a company to submit samples of each batch of the bulk product and the finished product fo…
Pharmacovigilance is carried out :1° For medicinal products and for products which must be covered by the marketing authorisation provided for in article L. 5121-8, after this authorisation has been i…
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