Article L5321-1
The Agency is subject to an administrative, budgetary, financial and accounting system and to State control adapted to the specific nature of its mission, as defined in this Book and specified by decr…
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Showing 8191–8200 of 63953 articles for “Art. L 312-19 and L 312-20”
The Agency is subject to an administrative, budgetary, financial and accounting system and to State control adapted to the specific nature of its mission, as defined in this Book and specified by decr…
The agency's resources are made up of :1° A subsidy from the State ;2° Subsidies from other public authorities, their public establishments, social security bodies, the European Union or international…
Failure by a wholesaler-distributor to comply with the public service obligations defined in application of article L. 5124-17-2 is punishable by two years' imprisonment and a fine of €150,000.
The following constitutes a breach subject to a financial penalty: 1° Failure by a marketing authorisation holder or a pharmaceutical company exploiting a medicinal product to constitute the safety st…
Attempts to commit the offences referred to in article L. 5439-1 shall be subject to the same penalties.
I.-A fee is payable by the applicant for the performance by the Agency of the following operations: 1° Analysis of samples and evaluation of the documentation relating to the control protocol submitte…
For the criminal offences mentioned in this chapter, natural persons are also liable to the following additional penalties: 1° Display or dissemination of the decision handed down, under the condition…
Failure to comply with a ban on the export of a medicinal product issued by the Agence nationale de sécurité du médicament et des produits de santé in application of article L. 5124-11 is punishable b…
Failure to comply with the rules on advertising for pharmaceutical companies and establishments laid down by decree in the Conseil d'Etat in accordance with the provisions of article L. 5124-18 is pun…
Failure by a sponsor, either within the two-month period preceding the clinical trial or when a substantial amendment to the trial is made, to send the Agency the information required by law relating…
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