- Guidelines for the conduct of clinical trials in Uganda
- Guidelines on Good Clinical Practice in the conduct of Clinical Trials involving human participants
- Guidelines on good manufacturing practice for medicinal products part I – basic requirements for medicinal products
- Guidelines on good manufacturing practice for medicinal products part II – basic requirements for active pharmaceutical ingredients
- Guidelines on good manufacturing practice for medicinal products
- Guidelines on licensing of class C Drug shops
- Guidelines on licensing of Pharmacies and Pharmaceutical Manufacturers
- Guidelines on the verification of applications for the importation and exportation of drugs and pharmaceutical raw and packaging materials
- Guidelines on competence profile of supervising pharmacists for a pharmaceutical manufacturing facility
- Guidelines on the conduct of clinical trials in children, pregnant and lactating women in Uganda
- Guidelines on the review and consideration of applications for monitored emergency use of unregistered and experimental interventions and off-label products for use in Uganda
- Guidelines on variations to registered pharmaceutical products
- Guidelines on registration of similar Biotherapeutic products
- Guidelines on registration of Biotherapeutic products
- Guidelines on registration of Human vaccines
- Guidelines on variation of registered Biotherapeutic products
- Submission of documentation for registration of a pharmaceutical product for human use
- Guidelines on Registration of Imported Herbal medicinal products for Human or Veterinary use
- Guidelines on hand sanitizers for use during the COVID-19 pandemic
- NDA insurance cover Guidelines
- Guidelines for detecting and reporting ADR
- Guidelines for Variation of Registered Vaccines
- Guidelines for Renewal of Registration of a Pharmaceutical product
- Guidelines for Adverse Events Following Immunization (AEFI)
- Guidelines on Periodic Safety Update Reports_R0
- Guidelines on Good Distribution Practice for Pharmaceutical Products
- Guidelines for introducing a new formulation pharmaceutical product on the Uganda market
- Guidelines for recall of a medical product
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- About Us
- Downloads
- DIRECTORATES
- Directorate of Inspectorate & Enforcement Services
- Directorate of Product Assessment & Registration
- Directorate of Product Safety
- Directorate of Corporate Services
- Directorate of Laboratory Services
- Directorate of Human Resource & Administration
- Directorate of Veterinary Services
- Office of the Secretary to the Authority
- REGISTERS
- Contact Us
Human Medicine Guidelines
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