Article R5132-44-1
When they are included in lists I or II, substances and preparations other than those mentioned in section 1 are subject to the provisions of articles R. 5132-1 to R. 5132-26.
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Showing 2831–2840 of 43182 articles for “Art. s. R 622-4”
When they are included in lists I or II, substances and preparations other than those mentioned in section 1 are subject to the provisions of articles R. 5132-1 to R. 5132-26.
Where the pharmacist dispenses contraceptives pursuant to article R. 5134-4-1 : 1° He may not, in application of article R. 5132-12 and under the conditions set out in paragraph 1 of article R. 5132-1…
I.-The register of purchases and sales provided for in article L. 225-211 to report transactions carried out pursuant to II of article L. 228-12 and of the I of article L. 228-12-1 is held under the t…
Only the following are authorised to record or modify the data mentioned in article R. 232-41-3:1° For the data mentioned in 1° to 3° of article R. 232-41-3, the agents of the testing department of th…
The samples referred to in the second paragraph of Article R. 1232-4-1 are taken in accordance with protocols issued by the Agence de la biomédecine. These protocols determine in particular the situat…
The committee meets at least twice a year, convened by its chairman, on his or her own initiative or, within a maximum of two months, at the written request of the full representatives of this committ…
Without prejudice to the case where the number of units prescribed corresponds to the number of units appearing in an initial outer packaging that complies with the provisions of article R. 5121-138,…
I.-Any healthcare professional who observes or is aware of a serious adverse reaction occurring in a blood donor shall report it without delay to the haemovigilance and transfusion safety corresponden…
If adverse reactions observed in a blood donor or in a recipient are likely to be due to a product mentioned in II of article L. 5311-1 falling within the scope of another vigilance, a copy of the adv…
I. - Any healthcare professional who observes or is aware of an adverse reaction occurring in a recipient of labile blood products shall report it without delay to the haemovigilance and transfusion s…
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