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Showing 4271–4280 of 34669 articles for “Art. R 418-9”
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…
Any supplier of particle accelerators or electrical equipment emitting ionising radiation must keep an up-to-date list of transfers of the equipment it has distributed. This list includes the nature a…
I.-Any holder of radioactive sources, accelerators or electrical equipment emitting ionising radiation subject to one of the regimes mentioned in Articles L. 1333-8 or L. 1333-9 shall have an inventor…
The results of the periodic inspections are recorded in the safety register(s) referred to in Article L. 4711-5.
When periodic inspections are carried out by persons not belonging to the establishment, the reports drawn up following these inspections are appended to the safety register. Failing this, precise det…
Periodic checks are carried out by qualified persons, who may or may not belong to the establishment, a list of whom is made available to the Labour Inspectorate. These persons have the necessary skil…
The safety register and reports may be kept and stored on any medium under the conditions set out in Article L. 8113-6.
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