Article R5121-176
…e L. 5126-1 shall forward to the Director General of the Agence nationale de sécurité du médicament et des produits de santé, immediately upon request, a report summarising the information relating to…
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Showing 5271–5280 of 40360 articles for “Art. R. 512-46-25 et s.”
…e L. 5126-1 shall forward to the Director General of the Agence nationale de sécurité du médicament et des produits de santé, immediately upon request, a report summarising the information relating to…
The procedures and standard form for the declarations and report mentioned in Articles R. 5121-174 to R. 5121-176 are laid down by decision of the Director General of the Agence nationale de sécurité…
For the application of Article R. 5127-13, where, due to the circumstances that led to the sample being taken or the appearance of the sample, as the case may be, the Director General of the Agence na…
When an exposure is not justified within the meaning of articles R. 1333-46 and R. 1333-47 but appears necessary for a patient in a particular case, the person requesting the procedure and the person…
Subject to the provisions of article R. 5126-46, the pharmacist responsible for managing the internal use pharmacy is appointed by the legal representative of the managing legal entity. In the case of…
…11-1 of the Consumer Code are not required to provide proof of the approval provided for in Article R. 331-25 in order to refer a matter to the Autorité de régulation de la communication audiovisuelle…
…the authorisation holder to the Director General of the Agence nationale de sécurité du médicament et des produits de santé, no later than six months before its expiry date. Any renewal of authorisat…
Failure to provide Pôle emploi with a statement of assignment contracts within the time limit set out in article R. 1251-7, in breach of the provisions of article L. 1251-46, is punishable by a third-…
…oducts of the human body mentioned in the first paragraph are intended for the manufacture of proprietary medicinal products or industrially manufactured medicinal products.
…sing, when these products are intended for the manufacture of in vitro diagnostic medical devices meeting the requirements to which they are subject for their marketing.The manufacturers concerned mus…
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