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Showing 4541–4550 of 24518 articles for “Art. CA Reims – 4 Oct. 2010”
When, as part of its inspection powers, the Agence nationale de sécurité du médicament et des produits de santé finds that the manufacture or repackaging and relabelling for distribution of raw materi…
…provisions of this book and of Book II of Part Four of this Code or of those adopted for their application, the authorisation may, after formal notice, be either suspended or withdrawn by the Director…
The procedures for applying this chapter, in particular the minimum information that e-commerce websites must contain, shall be determined by decree of the Conseil d'Etat.
…icinal products to a person established in France, medicinal products mentioned in article L. 5125-34 and benefiting from a marketing authorisation in France pursuant to article L. 5121-8 or one of th…
The Agence nationale de sécurité du médicament et des produits de santé publishes the principles of good laboratory practice applicable to non-clinical safety studies intended to assess the safety of…
The remit of some of the inspectors mentioned in Article L. 5127-1 may, where necessary, be extended to certain regions.
…sed in the absence of an appropriate authorised medicinal product available for the species and indication considered within the framework provided for in Articles 112 to 115 of Regulation (EU) 2019/6…
The advertising of certain medical devices and their accessories which present a significant risk to human health and whose list is set by order of the Minister for Health is subject to prior authoris…
Non-clinical trials intended to assess the properties and safety of medicinal products for veterinary use must comply with good laboratory practice, the principles of which are laid down by decision o…
In the cases provided for in articles L. 5145-2-1 and L. 5145-2-2 as well as in the case of suspension or withdrawal of a marketing authorisation or registration of a veterinary medicinal product, the…
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