I. – An order of the Minister for Health and the Minister for Defence, issued on a proposal from the Director General of the Agence nationale de sécurité du médicament et des produits de santé, specifies the procedures for submitting applications for approval and for amending the approvals provided for in III and VI of article L. 1222-11, as well as the content of the file accompanying each application.
II. – The decision of the Director General of the Agence nationale de sécurité du médicament et des produits de santé on the application for authorisation is taken within three months of the date of receipt of the application accompanied by a complete file. If no response is received by the end of this period, approval is deemed to have been refused.
III. – The decision granting the approval provided for in III and VI of Article L. 1222-11 specifies which of the transfusion activities mentioned in Article L. 1222-12 may be carried out by the Etablissement Français du Sang, by the blood establishment or by the armed forces blood transfusion centre, as well as the sites of the establishment where these activities may be distributed.