Article R522-24-1
The platform manager who keeps the register referred to in Article L. 522-37-1 establishes the rules for the operation of this register and the conditions for the issue of storage receipts by general…
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Showing 5931–5940 of 21427 articles for “Art. Cass. com. 31 March 2004”
The platform manager who keeps the register referred to in Article L. 522-37-1 establishes the rules for the operation of this register and the conditions for the issue of storage receipts by general…
When the Autorité de contrôle prudentiel et de résolution receives a request pursuant to II of Article L. 613-32-1 that a branch of a Class 1a credit institution or investment firm referred to in Arti…
For the organisation and operation of the High Council, its Chairman: 1° Represents the High Council in legal proceedings and acts on its behalf; 2° Appoints to posts, sets remuneration and compensati…
I.-The notification referred to in III of article L. 3512-17 includes the following information: 1° A detailed description of the product and instructions for its use; 2° The information on the ingred…
The sponsor shall provide the investigators of chemical, pharmaceutical, biological, pharmacological or toxicological tests with:1° The title and objective of the test requested ;2° Identification of…
Except where there are public health reasons for not doing so, parallel import authorisation is granted if the following conditions are met: 1° The proprietary medicinal product is obtained from an au…
As part of the pharmacovigilance system, any company or organisation exploiting a medicinal product or a product mentioned in Article R. 5121-150 : 1° Implements a risk management system for each medi…
Without prejudice to the obligations laid down in Articles R. 5121-138 to R. 5121-142, the packaging of a blood-derived medicinal product includes three detachable labels, separate from the informatio…
Veterinary pharmacovigilance includes : 1° The reporting of adverse reactions to veterinary medicinal products and medicinal products for human use administered under the conditions provided for in a…
For the purposes of placing on the market in vitro diagnostic medical devices other than those subject to a performance evaluation, manufacturers shall follow the following procedures: 1° For in vitro…
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