Article R2333-120-66
Where a decision of the Commission is vitiated by a material error likely to have had an influence on the judgment of the case, the interested party may appeal to the Commission for rectification.This…
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Showing 391–400 of 13064 articles for “Art. CE 9-12-2022 n° 459206”
Where a decision of the Commission is vitiated by a material error likely to have had an influence on the judgment of the case, the interested party may appeal to the Commission for rectification.This…
When the application is registered, the Chairman of the Commission appoints the rapporteur responsible for investigating the application.
…ea of public policy, the judge shall inform the parties thereof by any means that allows proof of receipt of this information by the addressees and shall set a time limit within which they may, withou…
…names of the claimant, a statement of the subject of the claim and the legal and factual circumstances invoked in writing in support of it and, if applicable, a mention of the written observations of…
…ned and cannot be appealed.This decision shall be communicated by any means allowing proof of its receipt by the addressees.Briefs that may have been produced during the period between the closure and…
If it appears from the application that the case is already certain to be resolved, the magistrate responsible for investigating the case may decide that there are no grounds for an investigation.
The operative part of the decisions is divided into articles and preceded by the word: "decides" or, where appropriate, "orders".The commission's decisions are enforceable.
…125-12-1 and L. 7227-12-1, is determined on the basis of the gross annual amount of official allowances received by local elected representatives, including the various increases provided for in artic…
In wastewater agglomerations whose population and economic activities produce wastewater with a gross organic pollution load of less than or equal to 120 kg per day, the treatment mentioned in article…
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…
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