This technical brief highlights MTaPS’ support to Mozambique’s Ministry of Health to successfully develop and implement a safety monitoring system for the newly-introduced Tenofovir/Lamivudine/Dolutegravir (TLD) antiretroviral […]
Read MoreThe process of product registration or marketing authorization is a key regulatory function of a national medicines regulatory authority (NMRA) to ensure the safety, quality, and […]
Read MoreThis report summarizes USAID MTaPS’ achievements, key challenges, program performance, and adaptation in response to new demands and lessons learned for the January through March 2022 […]
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