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Showing 11–20 of 37646 articles for “Art. L 1221-20”
I.-For the application of the provisions of sections 1 to 4 of this chapter, army hospitals and the army blood transfusion centre are, except in the case of external operations, considered respectivel…
The authorisation to manage a blood depot referred to in article L. 1221-10 is granted by the regional health agency with territorial jurisdiction, after obtaining the opinion of the Etablissement fra…
To be authorised, a blood depot must meet the following conditions: 1° Have an organisation and resources enabling it to carry out its activities in accordance with the procedures defined by order of…
Blood banks are subject to at least one inspection by the regional health agency during the period of validity of the authorisation.
For the application of this section, the Minister of Defence shall exercise the powers conferred on the competent regional health agency for army hospitals, whose technical opinion he may seek if nece…
I.-The refusal of authorisation to manage a blood establishment, its renewal or the substantial modification of one of its elements is notified to the director of the health establishment or to the ad…
The trial period lengths set by articles L. 1221-19 and L. 1221-21 are mandatory, with the exception of :-shorter periods set by collective agreements concluded after the date of publication of the af…
Advertising for the substances mentioned in article L. 1221-2 is prohibited. Medical information and information intended to indicate the location of depots do not constitute advertising. By way of de…
A decree of the Conseil d'Etat shall determine :1° The conditions under which the pre-employment declaration is made ;2° The procedures for recovery of the penalty provided for in article L. 1221-11.
Blood and blood components may be used for research purposes, whether or not they have been collected by the Etablissement Français du Sang. In this case, the research is carried out using samples tak…
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