Article 33 Application for authorisation or amendment of an authorisation

a list of intended uses F2and the competent authorities to whom the applicant has made or intends to make an application;

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

where relevant, a copy of any authorisations already granted for that plant protection product F4by a competent authority;

where relevant, a copy of any conclusion of the F5competent authority assessing equivalence as referred to in Article 38(2).

for the plant protection product concerned, a complete and a summary dossier for each point of the data requirements of the plant protection product;

for each active substance, safener and synergist contained in the plant protection product, a complete and a summary dossier for each point of the data requirements of the active substance, safener and synergist;

for each test or study involving vertebrate animals, a justification of the steps taken to avoid animal testing and duplication of tests and studies on vertebrate animals;

the reasons why the test and study reports submitted are necessary for first authorisation or for amendments to the conditions of the authorisation;

where relevant a copy of the application for a maximum residue level as referred to in Article 7 of Regulation (EC) No 396/2005 or a justification for not supplying such information;

where relevant for an amendment of an authorisation an assessment of all information submitted in accordance with point (h) of Article 8(1);

a draft label.