Article R4126-11
Complaints and pleadings must, on pain of inadmissibility, be accompanied by copies in a number equal to that of the parties plus two. Where the parties attach documents in support of their claims and…
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Showing 2801–2810 of 64366 articles for “Art. L. 622-17 and L. 611-11”
Complaints and pleadings must, on pain of inadmissibility, be accompanied by copies in a number equal to that of the parties plus two. Where the parties attach documents in support of their claims and…
The Labour Advisor responsible, in companies or inter-company services, for initiating, studying and implementing social achievements decided by the Social and Economic Committee and the employer perf…
…rsonal transport, they are exempt from import authorisation under the conditions set out in article L. 5124-13. A sports team doctor who personally transports a medicinal product or who imports a medi…
…horised company within the meaning of Article 77 of Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human…
…the Agence nationale de sécurité du médicament et des produits de santé as provided for in articles L. 1123-8 and R. 1123-30 ; however, where the implementation of the research is of an urgent nature,…
The proprietary medicinal product for which parallel import authorisation is sought may differ from the proprietary medicinal product which has already obtained marketing authorisation in France, as r…
…s obtained marketing authorisation in France, except that it includes : 1° The addition of the name and address of the establishment responsible for changing the packaging, in addition to the informat…
…plication for an import authorisation must be sent by any means capable of providing a date certain and must indicate : 1° The name or business name and address of the natural or legal person responsi…
The labelling and outer packaging of the proprietary medicinal product benefiting from a parallel import authorisation are identical to those of the proprietary medicinal product which has obtained ma…
…fused on expiry of a period of forty-five days from the date of receipt of the complete application and dossier referred to in Articles R. 5121-111 and R. 5121-112. The time limit mentioned in the pre…
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