Article Annexe II-16-2 (art. A212-217)
Aptitude test1. Test to verify theoretical and practical safety knowledgeThe purpose of the test to verify theoretical and practical safety knowledge is to verify, by means of an interview and on the…
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Showing 5131–5140 of 47964 articles for “Art. s. R 611-13 to R 611-16”
Aptitude test1. Test to verify theoretical and practical safety knowledgeThe purpose of the test to verify theoretical and practical safety knowledge is to verify, by means of an interview and on the…
Aptitude test 1. Test to verify theoretical and practical knowledge of safety. This test aims to verify the candidate's ability to design a mountaineering project based on their professional experienc…
Conditions for exploration in air diving in the natural environmentSPACESSUPERVISED DIVINGSCUBA DIVINGMinimum skillsof supervised diversMaximum numberof the group(not including the person supervisingt…
Conditions for teaching air diving in the natural environmentSURVEY AREASMINIMUM DIVER SKILLSSKILLSminimum of the person supervising the groupMAXIMUM NUMBERof the group(not including the person superv…
With regard to the transport undertakings listed at the end of article L. 611-4, the powers conferred by the provisions of this section, either on the Minister responsible for labour, or on the region…
The regional pharmacovigilance centres inform the Agence nationale de sécurité du médicament et des produits de santé on the same day of the reports of adverse reactions likely to be due to a blood-de…
Blood establishments and organisations or companies manufacturing or exploiting blood-derived medicinal products which are aware of information likely to cast doubt on the quality of blood or plasma i…
The correspondent mentioned in article R. 5121-181 who receives the report provided for in article R. 5121-196 immediately forwards it to the regional pharmacovigilance centre. If he is otherwise awar…
Organisations or companies exploiting blood-derived medicinal products which have knowledge of adverse reactions likely to be due to these medicinal products inform the Director General of the Agence…
When a person authorised to prescribe, dispense or administer medicinal products becomes aware of an adverse reaction which may be due to a blood-derived medicinal product, he/she shall report it imme…
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