Article L517-5
…511-52, L. 511-53, L. 533-25, L. 533-26, L. 533-27 and the regulatory texts adopted for their application. They shall also ensure that their subsidiaries properly apply the governance provisions set…
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Showing 4061–4070 of 34876 articles for “Art. CA Douai 4-5-2023 n° 22/00072”
…511-52, L. 511-53, L. 533-25, L. 533-26, L. 533-27 and the regulatory texts adopted for their application. They shall also ensure that their subsidiaries properly apply the governance provisions set…
…egard to the dose assessed pursuant to 4° of Article R. 4451-53, the employer shall classify as: 1° Category A, any worker likely to receive, over a period of twelve consecutive months: a) An effectiv…
…ner wishing to act as coordinating doctor must submit a request to the public prosecutor. This application must be accompanied by the following information and documents: 1° Nature of professional act…
…rised to continue practising the profession of hearing aid acoustician: 1° Persons holding a certificate of technical studies in acoustics applied to hearing aid fittings issued by faculties of medici…
…artment or by joint order of the State representatives in the departments concerned in the opposite case : 1° Either, within a period of two months from the first deliberation transmitted, on the init…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé may, by a reasoned decision setting out the appeal procedures and deadlines, automatically vary, suspend…
…hich must be mentioned in the risk management system are, in particular, the following: 1° The applicant must complete a trial programme within a period set by the Agency, the results of which will be…
The marketing authorisation is renewable on application by the holder to the National Agency for the Safety of Medicines and Health Products no later than nine months before its expiry date. The appli…
In the case of blood-derived medicinal products, the Agence nationale de sécurité du médicament et des produits de santé may, when examining the application for marketing authorisation, submit samples…
When, on the occasion of the implementation of Article 20(4) of Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004, urgent action is essential to protect human…
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