Article L947-4
…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…
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Showing 2721–2730 of 25314 articles for “Art. 4° bis”
…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…
…2° Information on the removal of tissues and cells; 3° Information on the preparation process used; 4° Information on the finished product; 5° List of products and materials coming into contact with t…
…igations and specifies the conditions of transport and intermediate storage of these raw materials; 4° The manufacturers of medicated feedingstuffs mentioned in 11° of article R. 5142-1 may subcontrac…
…l median of median incomes;3° The unemployment rate of the commune is higher than the national rate;4° 70% of the population of each public inter-communal cooperation establishment lives in communes f…
…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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