Advanced therapy medicinal products prepared on an ad hoc basis are distributed, under the responsibility of the person in charge referred to in article R. 4211-37 or, where applicable, the person in charge of site activities referred to in the same article, to an identified practitioner, on the basis of a named medical prescription.
They may only be distributed if they are recognised as complying with the health safety rules adopted in application of Article L. 1211-6, if they have been prepared and stored in accordance with the rules of good practice provided for in Article L. 5121-5 and if they are recognised as complying with the requirements mentioned in the authorisation granted in application of Section 17 of Chapter I of Title II of Book I of Part Five of the Public Health Code.