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Showing 6431–6440 of 49021 articles for “Art. CA Paris 6-2-2023 n° 21/10189”
…ng hybrid group may, by decision of the Director General of the Agence nationale de sécurité du médicament et des produits de santé, be entered in the register of hybrid groups in the same group, unti…
When the application for early access authorisation concerns a medicinal product composed, in whole or in part, of genetically modified organisms, the holder of the exploitation rights, or his authori…
…uthorisation is issued or varied by the Director General of the Agence nationale de sécurité du médicament et des produits de santé within thirty days of notification of the agreement by the reference…
The decision to refuse registration is notified to the training provider by the Regional Prefect within thirty days of receipt of the declaration and supporting documents. If no response is received w…
Dispensing chemists may supply shipping companies operating ships with medicines listed on the medical supplies provided for in the regulations annexed to the decree of 23 November 1987 relating to sh…
The dispensing of medicinal products prescribed on a conditional dispensing prescription referred to in article L. 5121-12-1-1 must comply with all the information contained therein.
…intended purpose of the product, its usual use or its instructions for use, or with the special precautions for use mentioned in 7° of article R. 513-10-5; Adverse reaction": a noxious and unintended…
…sion of the European Commission, the Director General of the Agency may, at the request of the applicant, grant a marketing authorisation. Once this decision has been taken, the authorisation may, if…
The declarations provided for in Articles L. 5211-3-1 and R. 5211-65 as well as the communication provided for in Article R. 5211-66 are made to the Agence nationale de sécurité du médicament et des p…
The certificate is issued by the person responsible for transferring the second-hand medical device to the transferee.
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