By way of derogation from Article 20(1) of Regulation (EU) No 528/2012 and the information requirements in Article 43(1) thereof, an application for authorisation of a same product shall contain the following information:
(a)the authorisation number or, for not yet approved related reference products, the application number in the Register for Biocidal Products of the related reference product;
(b)an indication of the proposed differences between the same product and the related reference product, and evidence that the products are identical on all other aspects;