- Registration of a Pharmaceutical product for Veterinary use in Uganda
- Veterinary Adverse Event Reporting Form
- Format for CTD cover letter for Veterinary pharmaceutical products
- Format for letters of access to APIMF and CEP for Veterinary pharmaceutical products
- Format for quality overall summary – product dossier (QOS-PD) for Veterinary products
- Template for quality information summary (QIS) for Veterinary Pharmaceutical Products
- Template for the summary of product characteristics for Veterinary Pharmaceutical products
- Application form for registration of a drug for Veterinary use
- Letter for Ectoparasiticide Trial Authorization from Manufacturer
- Information to be given to the Contracted Research Organisation to aid them in developing the Ectoparasiticide Trial Protocol
- Sample Interim or End of Ectoparasiticide Study Summary Report
- Format for Ectoparasiticide Trial Study Reports
- Format for Declaration by the Investigators for the Ectoparasiticide Trial
- Format for the Ectoparasiticide Trial Protocol
- The Contracted Research Organization Administrative Information for the Ectoparasiticide Trial
- The Ectoparasiticide Trial Application Format (ETAF)
- Required Documents by the Authority Inspector at the Port of Entry for Conduct of Ectoparasiticide Trials
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- DIRECTORATES
- Directorate of Inspectorate & Enforcement Services
- Directorate of Product Assessment & Registration
- Directorate of Product Safety
- Directorate of Corporate Services
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- Directorate of Human Resource & Administration
- Directorate of Veterinary Services
- Office of the Secretary to the Authority
- Public Relations Unit
- REGISTERS
- Contact Us
Veterinary Medicine Forms
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