Article R5121-9-2
When a marketing authorisation is granted for a biological medicinal product which may be identified as a similar biological medicinal product, the Director General of the Agence nationale de sécurité…
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Showing 3261–3270 of 39546 articles for “Art. L 227-9”
When a marketing authorisation is granted for a biological medicinal product which may be identified as a similar biological medicinal product, the Director General of the Agence nationale de sécurité…
Decisions to include a medicinal product on the reference list of similar biological groups, to amend these decisions and to remove it from this list are published on the website of the Agence nationa…
In specific cases of interest to the European Union, the Director General of the National Agency for the Safety of Medicines and Health Products or the applicant shall refer the matter to the European…
Each société de participations financières de profession libérale de pharmaciens d'officine may be subject to occasional checks on the scope of its activities, as prescribed by the Conseil national de…
The modelling agency licence is issued for an indefinite period by the Prefect of Paris. The Ile-de-France Regional Director for Business, Competition, Consumer Affairs, Labour and Employment examines…
The members of the National Labour Inspection Council carry out their duties in compliance with the requirements of independence, impartiality and integrity. They are bound by the secrecy of the body'…
The Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail or the applicant for marketing authorisation may refer the matter to the European…
The application for authorisation to import a veterinary medicinal product in parallel is sent to the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environneme…
When a health care institution uses an external service provider mentioned in 4° of the I of article R. 6113-5 to implement the activities mentioned in this chapter, this service provider may not reta…
Records of all access, consultation, creation and modification of patient data are kept for a period of six months at a time by the health care organisation.Traces of actions carried out by the servic…
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