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Showing 8781–8790 of 59899 articles for “Art. R 134-1”
A member may, on condition that he informs the company by registered letter with acknowledgement of receipt, cease his professional activity within the company. He must comply with the deadline set by…
Testing of medicinal products, within the meaning of 9° of article L. 5121-20, means all chemical, pharmaceutical and biological tests, non-clinical tests and clinical trials. Without prejudice to the…
The investigational medicinal products and, where applicable, the devices used to administer them are supplied free of charge by the sponsor, except where the law provides otherwise.
The people who direct and supervise the performance of chemical, pharmaceutical, biological, pharmacological or toxicological tests are known as experimenters.
When the complaint involves one of the members of the body of the Order of Pharmacists in New Caledonia or French Polynesia, this body may ask the President of the National Council of the Order of Pha…
The standards and methods applicable to the testing of medicinal products are set, on a proposal from the Director General of the Agence nationale de sécurité du médicament et des produits de santé, b…
Investigational medicinal products are prepared in accordance with the good practices mentioned in article L. 5121-5. The information appearing on the labelling must be written at least in French. The…
The regional directorate for youth, sport and social cohesion provides the committee's secretariat.
Subject to the provisions of articles L. 1123-6 to L. 1123-8 and L. 1123-13 and those adopted for their application, the investigators and persons called upon to collaborate in the trials are bound by…
For finished products, defined as medicinal products that have undergone all stages of manufacture, including packaging, an import authorisation is required for each import operation. For medicinal pr…
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