Article L5125-1-1-1
The General Director of the Regional Health Agency shall suspend or prohibit the performance of preparations, other than those referred to in Article L. 5125-1-1, if the pharmacy does not comply with…
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Showing 4091–4100 of 68114 articles for “Art. R 123-38 · Cass. com. 17 February 2015 · C. com. Art. L 145-1”
The General Director of the Regional Health Agency shall suspend or prohibit the performance of preparations, other than those referred to in Article L. 5125-1-1, if the pharmacy does not comply with…
I.-The following nuclear activities are subject to the declaration, registration or authorisation system mentioned in Article L. 1333-8, subject to the provisions of Article L. 1333-9: 1° For radioact…
I. - The assets referred to in II of article L. 214-168 are financial instruments, receivables or any other asset within the meaning of article L. 214-154, or risk or cash sub-participations. Direct o…
When a commercial agent has assigned to his professional activity assets separate from his personal assets pursuant to the provisions of article L. 526-6, and transfers his domicile within the meaning…
The voting rights and dividend rights of shares or share fractions issued in breach of the provisions relating to the incorporation of public limited companies with a public offer, as set out in this…
I.- Subject to the adaptation provisions provided for in II, the articles mentioned in the left-hand column of the following table shall apply in the Wallis and Futuna Islands, in the wording indicate…
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…
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