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Regulation (EU) 2024/568 of the European Parliament and of the Council of 7 February 2024 on fees and charges payable to the European Medicines Agency, amending Regulations (EU) 2017/745 and (EU) 2022/123 of the European Parliament and of the Council and repealing Regulation (EU) No 658/2014 of the European Parliament and of the Council and Council Regulation (EC) No 297/95

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CELEX:  02024R0568-20240214

Types of fees and charges The Agency may levy the following types of fees or charges:
(a) fees and charges for assessment procedures and services relating to medicinal products for human use, as set out in Annex I;
(b) fees and charges for assessment procedures and services relating to veterinary medicinal products, as set out in Annex II;
(c) annual fees for authorised medicinal products for human use and for authorised veterinary medicinal products, as set out in Annex III;
(d) other fees and charges for medicinal products for human use, veterinary medicinal products and consultations on medical devices, as set out in Annex IV.