For active substances which were re-included in Annex I from 1/1/2016, the authorisation holders of products based on these active substances need to submit renewal requests for all of these products, as specified by article 43 of Regulation 1107/2009.

You can find practical information regarding this type of request in our guide and in the guidance document for renewals under article 43.

Following the re-inclusion of the active substance, all authorisation holders will also receive instructions from our service, which once again explains which steps must be followed if the authorisation holder wishes to retain their authorisation.