Article R5121-154
…ompanies and organisations exploiting a medicinal product or a product mentioned in Article R. 5121-150 ; 2° Reports sent by companies and organisations exploiting medicinal products or products menti…
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Showing 1411–1420 of 4596 articles for “Art. 15 Oct 1997”
…ompanies and organisations exploiting a medicinal product or a product mentioned in Article R. 5121-150 ; 2° Reports sent by companies and organisations exploiting medicinal products or products menti…
…ny company or organisation exploiting a medicinal product or a product mentioned in article R. 5121-150 which has reported a suspected adverse reaction in application of the provisions of article R. 1…
The regional pharmacovigilance centres carry out vigilance missions relating to health products under the conditions defined in article R. 1413-61-4.
…ny company or organisation exploiting a medicinal product or a product mentioned in article R. 5121-150, that, due to their concerns regarding the safety of a medicinal product, the marketing of the m…
…noxious and unintended response to a medicinal product or to a product mentioned in Article R. 5121-150 ; 2° "Serious adverse reaction": an adverse reaction which is lethal or life-threatening, or whi…
…erse reactions suspected to be due to a medicinal product or a product mentioned in article R. 5121-150, including cases of overdose, misuse, abuse and medicinal errors as defined in article R. 5121-1…
Withdrawal of the approval provided for in the third paragraph of Article L. 5122-9 is decided by the Director General of the Agence nationale de sécurité du médicament et des produits de santé after…
The suspension, which may not exceed one year, and the withdrawal of the authorisation to open, provided for in article L. 5124-3, are decided by the Director General of the Agence nationale de sécuri…
A société d'exercice libéral de pharmaciens d'officine is formed subject to the condition precedent that it is entered on the roll of the ordre under the conditions set out in articles R. 4222-1 et se…
The premises are installed and equipped in such a way as to ensure the proper storage, monitoring and, if necessary, withdrawal of the medicinal products, products or articles mentioned in Articles L.…
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