A copy of the report or record of sampling shall be sent by its author(s), as appropriate, to the Director General of the Agence nationale de sécurité du médicament et des produits de santé or to the Director General of the Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail.
The Agency will immediately inform the officials who drafted the report or the minutes whether it is the recipient of the samples taken, specifying which of its laboratories is responsible for carrying out the analyses or, where appropriate, the specialised establishment or body designated for this purpose. In the latter case, a copy of the report or record is also sent by its author(s) to this establishment or body at the same time as the samples.