Article R5121-109
For finished products, defined as medicinal products that have undergone all stages of manufacture, including packaging, an import authorisation is required for each import operation. For medicinal pr…
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Showing 951–960 of 24512 articles for “Art. Cass. 1ère civ. 20-10-2010 n° 09-13.635 FS-PBI”
For finished products, defined as medicinal products that have undergone all stages of manufacture, including packaging, an import authorisation is required for each import operation. For medicinal pr…
Where warranted by an emergency situation, in particular that described in Article 18 of Regulation (EU) No 1093/2010, or an adverse development that is likely to threaten market liquidity or the stab…
Non-substantial modifications must be declared to the regional health agency. A copy is sent to the Etablissement français du sang or, where applicable, to the Centre de transfusion sanguine des armée…
Mediators are set up in order to promote, without prejudice to the right of the parties to take legal action, the resolution of disputes relating to the granting of the authorisation for simultaneous,…
I.-The application for an initial authorisation to manage a blood establishment is sent by the director of the health establishment or by the administrator of the grouping to the regional health agenc…
The pharmaceutical record is closed by the Conseil national de l'ordre des pharmaciens when the holder so requests under the conditions set out in article R. 1111-20-6. When the Conseil national de l'…
I. - When, as the authority responsible for supervision on a consolidated basis, the Autorité de contrôle prudentiel et de résolution receives an application for authorisation to use an internal risk…
When they market structured deposits within the meaning of Article L. 312-22 or when they provide advice on these deposits, credit institutions are subject to the provisions of 2°, 3° and 6° of II of…
I.-The persons referred to in Article L. 561-2 shall define and implement procedures enabling them to determine whether the transaction they are carrying out is one of those referred to in 3° of Artic…
The French Anti-Doping Agency is entitled to receive from a body recognised by the World Anti-Doping Agency and having similar competencies to its own, information of the nature mentioned in the first…
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