Article R1511-16
In the regional aid areas delimited by the decree mentioned in article R. 1511-10, local authorities and their groupings may grant aid for business property investment under the conditions set out in…
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Showing 1571–1580 of 57450 articles for “Art. L 123-16-2”
In the regional aid areas delimited by the decree mentioned in article R. 1511-10, local authorities and their groupings may grant aid for business property investment under the conditions set out in…
Examinations of equipment, machinery, installations or protective devices are repeated as often as necessary, in particular: 1° After each dismantling or modification, or when one of their parts has b…
The employer draws up an annual report on the implementation of the agreement and presents it to the social and economic committee or the group works council, as appropriate. The implementation of bra…
The training leading to the state diploma of masseur-physiotherapist, organised in two cycles of four semesters each, lasts four years, i.e. eight semesters. The training programme organises the devel…
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…
Any company or organisation exploiting a medicinal product or a product mentioned in Article R. 5121-150 shall implement a pharmacovigilance system in order to fulfil its pharmacovigilance obligations…
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…
Any company or organisation exploiting a medicinal product or a product referred to in Article R. 5121-150 has at its disposal on a permanent basis the services of a person responsible for pharmacovig…
The company or organisation exploiting a medicinal product or a product referred to in Article R. 5121-150 may not communicate information relating to pharmacovigilance to the general public about thi…
I.-Any company or organisation exploiting a medicinal product or a product mentioned in article R. 5121-150 is required to transmit electronically to the European Medicines Agency a periodic safety up…
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