Clinical Trials in Resource-Limited Settings

The goal of the Global Health Clinical Trials Programme is to promote and make easier the conduct of non-commercial clinical research across all diseases in resource-poor settings. We present a series of short lectures to provide an introduction to clinical trials and explore some of the challenges facing clinical trialists in resource-limited settings.

Tropical Medicine Department for Continuing Education

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Displaying 1 - 9 of 9 episodes

Episode	Description	People	Date
Occupational Health and Safety in a Research Setting	Dr Simon Ndirangu, Bioanalytical Laboratory at the Kenya Medical Research Institute (KEMRI)/Wellcome Trust Research Programme in Kilifi, Kenya discusses the importance of implementing occupational health and safety standards in research settings.	Simon Ndirangu Muchohi	29 October, 2009
Measurement of Drug Levels in Clinical Trials	Dr Simon Ndirangu, Bioanalytical Laboratory at the Kenya Medical Research Institute (KEMRI)/Wellcome Trust Research Programme in Kilifi, Kenya describes the basic concepts of pharmacological clinical trials, pharmacokinetics and pharmacodynamics.	Simon Ndirangu Muchohi	29 October, 2009
Setting Up a Laboratory for Clinical Trials in Resource-Poor Settings	Ken Awuondo, Clinical Trials Laboratory Manager for the Kenya Medical Research Institute (KEMRI)/Wellcome Trust Research Programme in Kilifi, Kenya gives an overview of the requirements for setting up a laboratory in resource-poor settings.	Ken Awuondo	29 October, 2009
The Role of Laboratory in Clinical Trials	Ken Awuondo, Clinical Trials Laboratory Manager for the Kenya Medical Research Institute (KEMRI)/Wellcome Trust Research Programme in Kilifi, Kenya gives an overview of the role of the laboratory in clinical trials.	Ken Awuondo	29 October, 2009
Data Safety Monitoring Boards: Their Place and Role in Trials	Dr Roma Chilengi, Head of Clinical Trials at the Kenya Medical Research Institute (KEMRI)/Wellcome Trust Research Programme in Kilifi, Kenya discusses clinical trial data safety monitoring boards (DSMBs).	Roma Chilengi	29 October, 2009
Clinical Trial Protocol Development	Dr Phaik Yeong Cheah, Head of Clinical Trials at the Mahidol-Oxford Research Unit in Bangkok, Thailand discusses clinical trial protocol development.	Phaik Yeong Cheah	29 October, 2009
Introduction to Research Ethics	Dr Roma Chilengi, Head of Clinical Trials at the Kenya Medical Research Institute (KEMRI)/Wellcome Trust Research Programme in Kilifi, Kenya gives an introduction to research ethics.	Roma Chilengi	29 October, 2009
The Story of ICH-GCP: An introduction for investigators and site staff	Dr Roma Chilengi, Head of Clinical Trials at the Kenya Medical Research Institute (KEMRI)/Wellcome Trust Research Programme in Kilifi, Kenya gives an introduction to ICH-GCP.	Roma Chilengi	29 October, 2009
An Introduction to Clinical Trials	George Warimwe from the Kenya Medical Research Institute (KEMRI)/Wellcome Trust Research Programme in Kilifi, Kenya presents an introduction to clinical trials aimed at trial site staff and anyone new to the field.	George Warimwe	29 October, 2009

Clinical Trials in Resource-Limited Settings

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