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Showing 4551–4560 of 69879 articles for “Art. I-1°-a”
The declarations and the periodic safety update report referred to in Articles R. 5121-161, R. 5121-168 and R. 5121-170 are drawn up in accordance with the procedures and standard form laid down by th…
Any company or organisation exploiting a medicinal product or a product mentioned in Article R. 5121-150 implements procedures to obtain accurate and verifiable information for the scientific evaluati…
The in-house pharmacies referred to in Article L. 5126-1 shall forward to the Director General of the Agence nationale de sécurité du médicament et des produits de santé, immediately upon request, a r…
The procedures and standard form for the declarations and report mentioned in Articles R. 5121-174 to R. 5121-176 are laid down by decision of the Director General of the Agence nationale de sécurité…
The Minister responsible for health shall determine: 1° By order issued on a proposal from the Agence de la biomédecine, the recommendations of good practice relating to the methods of access, care fo…
I.-Where a worker's exposure cannot be avoided by the use of collective protection measures, the employer shall provide appropriate and suitable personal protection equipment in order to reduce this e…
All pleas of nullity against procedural acts that have already been performed must be raised simultaneously, failing which those that have not been raised will be inadmissible.
No procedural act may be declared null and void on the grounds of a defect in form unless its nullity is expressly provided for by law, except in the case of failure to observe a substantial formality…
The nullity of procedural acts may be invoked as and when they are performed; but it is covered if the person invoking it has, subsequent to the act criticised, put forward defences on the merits or o…
The penalty for failure to observe a procedural formality prior to the hearing shall be subject to the rules laid down in this sub-section.
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