Human Medicine Guidelines

Part 1 GMP Guidelines for Medicinal Products_R3

2020-03-23

Part II GMP Guidelines for Medicinal Products (Basic Requirements for APIs)

2020-03-23

Annexes to GMP Guidelines for Medicinal Products_R2

2020-03-23

Guidelines on detecting & reporting adverse drug reactions in Uganda

2020-01-22

NDA insurance cover Guidelines

2019-10-23

NDA Guidelines on registration of Vaccines

2019-10-23

GUIDELINES-detecting and reporting ADR

2019-10-23

Guidelines for Variation of Registered Vaccines

2019-10-23

Guidelines for the conduct of clinical trials in Uganda

2019-10-23

Good Clinical Practice

2019-10-23

Guidelines for Renewal of Registration of a Pharmaceutical product

2019-10-23

Guidelines for Adverse Events Following Immunisation (AEFI)

2019-10-23

Guidelines for registration of Biotherapeutic products

2019-10-23

Guidelines of registration of Similar Biotherapeutic Products

2019-10-23

Licensing Guidelines 2019 Addendum - Gazette

2019-04-17

2019 Licensing Guidelines

2018-12-20

Guidelines on Periodic Safety Update Reports_R0

2018-04-12

Guidelines on Good Distribution Practice for Pharmaceutical Products

2018-04-12

Guidelines on Submission of Documentation for Marketing Authorisation of a Pharmaceutical Product for Human Use_R2

2018-02-06

Guidelines for Variation of Registered Medicinal Products_R2

2018-02-06

Guidelines for introducing a new formulation pharmaceutical product on the Uganda market

2018-01-23

 

NDA Guidelines_Control of Publication & Advertisment Relating to Drugs_R0

2017-08-17

Guidelines_Marketing Authorization of SRO-Approved Medicinal Products

2018-01-17

 

Guideline for recall of a medical product

2018-01-17