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Year 114 Clinical Research Participant Protection Course

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This course aims to provide personnel interested in participating in clinical trial projects with knowledge related to clinical trial research ethics and participant protection, informed consent, and adverse event reporting, as well as related learning points and precautions. It is recommended that current and future researchers planning human trial projects actively participate, attend the full session and verify attendance for a total of 6 hours, plus an additional 2 hours for completing the assessment.

Related registration information is attached.

https://forms.gle/75xP349bnp3TY5wP7

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