Article R5121-4
For any medicinal product authorised on the French market, each of its presentations and, where applicable, each common dispensing unit, is allocated a national identification number. This number is a…
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Showing 3561–3570 of 41745 articles for “Art. 4 mai 1994”
For any medicinal product authorised on the French market, each of its presentations and, where applicable, each common dispensing unit, is allocated a national identification number. This number is a…
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…
…ty and working conditions are governed by the provisions of Article 81, II of Article 83, Articles 84 and 85, II of Article 87, Articles 88 and 89, the first five paragraphs of Article 90, Articles 92…
I.-This article applies to the agreement mentioned in I of article L. 441-3 when it relates to mass-market products defined as non-durable products that are consumed frequently and repeatedly. The lis…
Manufacturers of veterinary medicinal products mentioned in 1° of article R. 5142-1 must justify, at all times, that all the products they use, manufacture and deliver comply with the characteristics…
…ystem, particularly, where applicable, with regard to sterilisation. The manufacturer undertakes to maintain his quality system in an appropriate and efficient manner and to fulfil the obligations ari…
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