Article L541-4
…the quality of this programme of operations in the light of the obligations set out in Articles L. 541-2, L. 541-3 and L. 541-8, as well as the conditions under which the financial investment adviser…
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Showing 2201–2210 of 24664 articles for “Art. 4 juin 1973”
…the quality of this programme of operations in the light of the obligations set out in Articles L. 541-2, L. 541-3 and L. 541-8, as well as the conditions under which the financial investment adviser…
…es, when they employ in the collectivity from two hundred to four hundred and ninety-nine employees;4° By four additional representatives, where they employ in the collectivity from five hundred to on…
I.-The application for authorisation provided for in Article L. 1243-2 shall be sent to the Director General of the Agence nationale de sécurité du médicament et des produits de santé by the legal ent…
The establishments mentioned in article R. 5142-1 may not subcontract any of the activities defined in the same article, subject to the exceptions mentioned below: 1° Manufacturers of veterinary medic…
…rning may only be issued if the damage has already been made good or if the measure provided for in 4° is also applied; 2° Referring the offender to a health, social or professional structure; this me…
Any breach of the provisions of articles L. 224-25-5 to L. 224-25-9 relating to the formation, modification and duration of the contract is punishable by an administrative fine of up to 3,000 euros fo…
…n Banking Authority ;3° The resolution authorities of the other Member States of the European Union;4° The competent authorities, within the meaning of Article 4(1)(40) of Regulation (EU) No 575/2013…
I.-Any healthcare professional who observes or is aware of a serious adverse reaction occurring in a blood donor shall report it without delay to the haemovigilance and transfusion safety corresponden…
If adverse reactions observed in a blood donor or in a recipient are likely to be due to a product mentioned in II of article L. 5311-1 falling within the scope of another vigilance, a copy of the adv…
I. - Any healthcare professional who observes or is aware of an adverse reaction occurring in a recipient of labile blood products shall report it without delay to the haemovigilance and transfusion s…
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