Protection of human research subject is crucial in clinical trials and should be carefully considered in every single step of a clinical trial. One important component in human subject protection is recruitment of potential clinical trial participants. In this article we reviewed the practical aspects of clinical trial subject recruitment from a human research protection perspective, considering the evolvement of relevant government guidance and regulations in Taiwan and latest global development as a result of advance in clinical trials methodology, changes in regulatory requirement in different countries, and utilization of information technology. We also made suggestions on practices of clinical trial teams and ethics review in Taiwan to support engagement in cutting edge clinical trials.
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