Registration of Veterinary Medicinal Products
- Preparation of veterinary medical product registration dossier in e-application format
- Updating the dossiers of existing registered products in accordance with the new regulation
- Preparation of Part 3 and Part 4 only (Part 1 C2 and 1 C3 expert report not included)
- Conducting the correspondence with the Ministry
- Preparation of Type I A, Type I B, Type II variation applications
- Preparation of Summary of Product Characteristics, Patient Information Leaflet, inner-outer label
- Registration renewal application
- Sales authorization application