Health professionals and manufacturers, importers, downstream users and distributors of substances or mixtures are required to provide, at the request of the bodies responsible for toxicovigilance, regional health agencies or the Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail, any additional information they may have on cases they have reported and on cases that have been reported by a third party. The organisations that receive this additional information ensure that it is recorded in the information system mentioned in article R. 1340-6 and ensure compliance with the provisions of articles R. 1340-6 and R. 1340-7.
This provision does not apply when the declaration comes under another vigilance system relating to products defined in articles L. 5311-1, L. 5141-1 and R. 1323-1.