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Accessed November, 2017
This guideline is intended to provide requirements to applicants wishing to submit applications for registration of medicines in Botswana.
Document No. : FDA/SMC/SMD/GL-SMP/2015/05 | These guidelines are for information, guidance and strict compliance by Marketing Authorization Holders and Local Representatives of regulated products to help in the continuous safety monitoring of products granted marketing authorization in Ghana.
Interim policy guidance.
Therapeutics Information and Pharmacovigilance Centre | TIPC
STATUTORY INSTRUMENTS | SUPPLEMENT No. 8 28th March, 2014 | STATUTORY INSTRUMENTS SUPPLEMENT | to The Uganda Gazette No. 18 Volume CVII dated 28th March, 2014 | Printed by UPPC, Entebbe, by Order of the Government. | STATUTORY INSTRUMENTS | 2014 No. 29.
Guidance for the preparation and submission of dossiers
First Edition
First Edition
A report submitted to the International Labour Organization, Geneva
Systematic screening for active tuberculosis: an operational guide.
Guidelines for Handling Temperature Sensitive Vaccines and Pharmaceuticals
This Global Plan builds on the previous edition, which laid out priority actions for 2018-2022, informed by global commitments member states endorsed at the 2018 United Nations High-Level Meeting (UNHLM) on TB. The resource needs estimates from this Global Plan include resources needed for implement ... more
Global Plan to end TB 2016-2020
DHS Working Papers No. 125