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Showing 1111–1120 of 3411 articles for “Art. BRDA 19/81”
The formalities of transcribing, recording and drawing up the forms provided for in this paragraph take the place of the transcriptions and recordings mentioned in article R. 5132-10.
When a healthcare professional administers a blood-derived medicinal product outside healthcare establishments or the establishments and organisations mentioned in article R. 5121-192, he/she affixes…
In blood transfusion establishments and in any organisation other than pharmacies, health establishments and health cooperation groups authorised to dispense blood-derived medicinal products, these me…
The correspondent mentioned in article R. 5121-181 who receives the report provided for in article R. 5121-196 immediately forwards it to the regional pharmacovigilance centre. If he is otherwise awar…
Organisations or companies exploiting blood-derived medicinal products which have knowledge of adverse reactions likely to be due to these medicinal products inform the Director General of the Agence…
When a person authorised to prescribe, dispense or administer medicinal products becomes aware of an adverse reaction which may be due to a blood-derived medicinal product, he/she shall report it imme…
All pharmaceutical acts are carried out under the effective control of a pharmacist who meets the conditions for practising pharmacy in France.
For a product mentioned in article L. 5122-14, the visa for advertising to the public mentioned in article L. 5122-8 is issued and may be suspended or withdrawn under the conditions set out in article…
The direct or indirect holding of shares representing all or part of the share capital of a société d'exercice libéral de pharmaciens d'officine by a natural or legal person practising a liberal healt…
Any debtor who disputes the undue nature of the benefits referred to in Articles L. 5422-1 and L. 5424-25 which are claimed from him or her must first submit an informal appeal to the Director General…
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