I.-The treatment products and processes used to comply with the rules laid down in Article D. 1332-2 are authorised by the Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail. If an application for authorisation to use these products and processes is not acted upon for more than six months, this is deemed to constitute a decision to accept it. An order by the Minister for Health defines the elements and procedures for submitting the application for authorisation.
II-The provisions laid down in I do not apply to biocidal products and processes authorised following a procedure for authorising their availability on the market pursuant to Regulation (EU) No 528/2012 of 22 May 2012.