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Clinical Trial Protocol Development

Series
Clinical Trials in Resource-Limited Settings
Dr Phaik Yeong Cheah, Head of Clinical Trials at the Mahidol-Oxford Research Unit in Bangkok, Thailand discusses clinical trial protocol development.
This lecture is an introduction to the topic and gives an overview from initial concept through to GCP requirements, ethical considerations, study drugs and procedures and safety reporting.

More in this series

View Series
Clinical Trials in Resource-Limited Settings

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).
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Clinical Trials in Resource-Limited Settings

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.
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Episode Information

Series
Clinical Trials in Resource-Limited Settings
People
Phaik Yeong Cheah
Department: Department for Continuing Education
Date Added: 29/10/2009
Duration: 00:34:09

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