The referring blood establishment sends the establishments mentioned in the first paragraph of article R. 1221-40, the information relating to 1° and 2° of the same article and, where applicable, 2° of article R. 1221-41.
Decisions by the Director General of the Agence nationale de sécurité du médicament et des produits de santé (French Agency for the Safety of Medicines and Health Products), taken after consultation with the Etablissement français du sang (French Blood Establishment) and the Armed Forces Blood Transfusion Centre, may specify the content of the information referred to in this article and lay down the procedures for its collection by these establishments or its transmission by the blood establishment.