Article R694-7
For the purposes of implementing Article L. 694-8, the mandataire de justice who does not follow the recommendations of the collective coordination programme shall inform the juge-commissaire of his r…
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Showing 2451–2460 of 37028 articles for “Art. Cass. com. – 13 May 1970”
For the purposes of implementing Article L. 694-8, the mandataire de justice who does not follow the recommendations of the collective coordination programme shall inform the juge-commissaire of his r…
The court shall rule on the application to dismiss the coordinator in chambers after having heard or given the opportunity to be heard the debtor, the coordinator, the insolvency practitioners concern…
The Institut de Radioprotection et de Sûreté Nucléaire is responsible for: 1° Managing the information and monitoring system for exposure to ionising radiation and organising the access required to ap…
A joint order of the ministers responsible for labour, radiation protection and agriculture shall determine: 1° With regard to the competent person in charge of radiation protection: a) The content an…
To be designated as a radiation protection advisor, the following is required: 1° For the person competent in radiation protection, a training certificate issued by a training body certified by a cert…
When, in the light of the results of individual dosimetric monitoring, the exposure of a worker has exceeded one of the dose limit values set in Article R. 4451-6, the Institut de Radioprotection et d…
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…
For the medicinal products mentioned in 1° of II of article L. 5121-12 and in II of article L. 5121-12-1, the obligations set out in article R. 5121-161 and articles R. 5121-166 to R. 5121-170 are car…
…problems identified. Once the corrective measures have been fully implemented, the entries recorded may be deleted.
Any company or organisation exploiting a medicinal product or a product mentioned in Article R. 5121-150 is required to: 1° Record all adverse reactions suspected of being due to a medicinal product o…
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