Article R8113-3-2
The right of access to documents or information provided for in Article L. 8113-5-1 is exercised by the labour inspectors referred to in Article L. 8112-1 in the course of their visits and investigati…
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Showing 9801–9810 of 33456 articles for “Art. al. 3”
The right of access to documents or information provided for in Article L. 8113-5-1 is exercised by the labour inspectors referred to in Article L. 8112-1 in the course of their visits and investigati…
For the application of the provisions of articles L. 124-8, L. 124-10, L. 124-13, L. 124-14 and the first paragraph of article L. 124-9 of the Education Code, the host organisation or educational esta…
…nsed, subject to their inclusion on the list established by the order provided for in Article L. 5123-8, for medicinal products which comply with the following packaging rules: 1° Either the medicinal…
The pharmacist must inform the woman concerned that this method of dispensing is non-renewable beyond 6 months and that she should consult a doctor or midwife if she intends to continue taking medicat…
Faeces are collected on the premises of the establishment or body referred to in Article L. 513-11-1. By way of derogation from the first paragraph, the collection of faeces may, in the context of res…
I. - Before issuing the authorisation applied for, the Director General of the Agence nationale de sécurité du médicament et des produits de santé (French National Agency for the Safety of Medicines a…
For the advertising mentioned in articles R. 5141-83 and R. 5141-84, the advertising texts and documents must be filed with the Director General of the Agence nationale de sécurité sanitaire de l'alim…
When the pharmacist or veterinary surgeon responsible for an establishment engaged in the manufacture, import or use of veterinary medicinal products, other than those subject to clinical trials, beco…
Assistant pharmacists or veterinary surgeons entrusted with the release of batches must have at least six months' professional experience under the conditions set out in article R. 5142-16 before taki…
…turer is required to update the risk analysis and management system referred to in Article R. 5211-23-2 by analysing all elements relating to the medical devices he manufactures and taking account of…
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