Gershom Chongwe on Muck Rack

Gershom Chongwe

As seen in: MDPI, Human Resources for Health, medRxiv
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Articles

High measles and rubella vaccine coverage and seroprevalence among Zambian children participating in a measles and rubella supplementary immunization activity

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By Christine Prosperi, Shaun Truelove, Gershom Chongwe, Phillimon Ndubani
| medRxiv
The authors have declared no competing interest. This serosurvey was supported by the Strengthening Immunization Systems through Serosurveillance grant (Grant number 1094816) from The Bill & Melinda Gates Foundation to the International Vaccine Access Center, Department of International Health, Johns Hopkins Bloomberg School of Public Health. I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
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Feasibility and acceptability of collecting dried blood spots (DBS) from children after vaccination during Supplementary Immunization Activities to estimate measles and rubella

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By Christine Prosperi, Gershom Chongwe, Mutinta Hamahuwa, Kelvin Kapungu
| medRxiv
The authors have declared no competing interest. This work was supported by the Strengthening Immunization Systems through Serosurveillance grant (grant number 1094816) from The Bill & Melinda Gates Foundation to the International Vaccine Access Center, Department of International Health, Johns Hopkins Bloomberg School of Public Health. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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Ethics of Adaptive Designs for Randomized Controlled Trials

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By Gershom Chongwe, Joseph Ali, Dan Kaye, Charles Michelo
| pericles.pericles-prod.literatumonline.com
Supporting Information The appendices are available in the “Supporting Information” section for the online version of this article and via Ethics & Human Research's “Supporting Information” page: https://www.thehastingscenter.org/supporting-information-ehr/. Filename Description eahr500178-sup-0001-S1.pdf737.2 KB Supporting Information REFERENCES 1, and , “The Real-World Ethics of Adaptive-Design Clinical Trials,” Hastings Center Report 47, no. 6 (2017): 27–37.
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