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Showing 2381–2390 of 57736 articles for “Art. s. 1133 and 13”
The mandate given pursuant to Article L. 1611-7-2 shall specify in particular: 1° The nature of the transactions to which the mandate relates; 2° The duration of the mandate and the conditions under w…
The provisions of this sub-section set out the accounting and financial terms and conditions for mandates entrusted pursuant to Article L. 1611-7-2.
The Director General of the Agence nationale de sécurité du médicament et des produits de santé: 1° Records any adverse reaction suspected to be due to a medicinal product or to a product mentioned in…
…é du médicament et des produits de santé shall fulfil its obligations in terms of pharmacovigilance and participation in European Union activities in this field.The National Agency for the Safety of M…
Without prejudice to the obligations laid down in Articles R. 5121-138 to R. 5121-142, the packaging of a blood-derived medicinal product includes three detachable labels, separate from the informatio…
…he person administering the blood-derived medicinal product to the patient completes the dispensing and administration slip with the following information: 1° The patient's surname, forenames and date…
…cy may ask the regional pharmacovigilance centres to carry out any pharmacovigilance investigations and work.He may also ask the drug dependence and addictovigilance assessment and information centres…
…This supply is managed in accordance with the provisions of the order provided for in article R. 5132-42. When a medicinal product is taken from the supply provided for in the previous paragraph, th…
…d in II to IV of this article. II.It informs the European Commission, the European Medicines Agency and the other Member States of the European Union of one of the following situations: 1° It is consi…
In health establishments and health cooperation groups authorised under article L. 6133-7 to carry out the tasks of these establishments which do not have an in-house pharmacy which hold blood-derived…
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