Article R232-41-10
The following documents and proceedings may be transmitted electronically, under conditions defined by the Agency: 1° The designation of athletes to form the Registered Testing Pool referred to in art…
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Showing 2781–2790 of 43476 articles for “Art. Art. R 210-4”
The following documents and proceedings may be transmitted electronically, under conditions defined by the Agency: 1° The designation of athletes to form the Registered Testing Pool referred to in art…
The provisions of article R. 752-36 are applicable. In the event that the matter has previously been referred to the National Commission by third parties, the latter shall have two months from notific…
A chain, rope or strap within the meaning of 5° of article R. 4311-4 is a chain, rope or strap designed and manufactured for lifting and forming part of a lifting machine or lifting accessory.
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…
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…
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