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Showing 5081–5090 of 25879 articles for “Art. CE 7-5-1986 n° 39426”
…lication of the classification rules between the manufacturer of an in vitro diagnostic medical device and an authorised body involved in the conformity assessment procedures provided for in this Titl…
The regional material vigilance and reactovigilance coordinators carry out their vigilance duties under the conditions defined in article R. 1413-61-4.
Prescriptions for medical devices issued at the request of a patient with a view to obtaining a supply in another Member State of the European Union must include the following information: 1° The surn…
…country information, to 3° of Article R. 5211-70, persons legally authorised to supply medical devices may refuse to supply these products, prescribed in another Member State of the European Union by…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé will notify the applicant of his decision on prior authorisation within two months of the date of receip…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé will notify the applicant of his prior authorisation decision within two months of the date of receipt o…
…of Part I and the regulatory measures taken for its application falling within the remit of the Agence nationale de sécurité du médicament et des produits de santé defined in Article L. 5311-1, the Ag…
…Directors are performed free of charge. Travel and accommodation expenses are reimbursed in accordance with the regulations applicable to civil servants.
…plasma mixtures intended for the manufacture of blood-derived medicinal products: €100; - of substances which, if used separately from a medical device in which they are incorporated as an integral pa…
…is ill or who has an incapacity or disability is cared for by the multidisciplinary team, the service provider and the equipment distributor will cooperate with the members of this team in the intere…
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