Article R5121-211
The application for authorisation is deemed to be complete if, within one month of receipt, the Director General of the Agence nationale de sécurité du médicament et des produits de santé has not info…
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Showing 3481–3490 of 56154 articles for “Art. 413-6 · C. com. Art. L 121-5 · Cass. 1re civ. 25 November 1986 · Cass. com. 21 October 2014 n° 13-22.428”
The application for authorisation is deemed to be complete if, within one month of receipt, the Director General of the Agence nationale de sécurité du médicament et des produits de santé has not info…
For the application of the provisions of this chapter, army hospitals and the army blood transfusion centre shall be regarded as health establishments and a blood transfusion establishment respectivel…
The Agence de la biomédecine is informed of the decisions taken in application of Article R. 5121-212.
The authorisation may be subject to special conditions requiring the beneficiary of the authorisation to implement a plan for monitoring the efficacy and safety of the medicinal product, including the…
Subject to the provisions of article R. 5125-24, the exclusion of a member of a société d'exercice libéral de pharmaciens d'officine may be decided, when he contravenes the operating rules of the comp…
The constraint is served on the debtor by registered letter with acknowledgement of receipt or by bailiff's deed. On pain of nullity, the bailiff's writ or the registered letter shall mention :1° The…
The medical file is completed at subsequent visits. At these visits, a new medical fitness form is drawn up and given to the employer and the employee under the same conditions as the initial medical…
A prescription for medicinal products in lists I and II may not be made for a treatment period of more than twelve months.However, for public health reasons, in the case of certain medicinal products,…
…isition and use of micro-organisms and toxins or products containing them in a form or under a name liable to cause confusion or to mislead as to their properties or dangerousness are prohibited.
The director, the administrator of the health cooperation group or the legal representative of the establishment defines, on a proposal from the chairman of the establishment's medical commission or t…
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