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2026 Human Research Ethics Course

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This course aims to provide personnel interested in participating in clinical trial projects with knowledge of clinical trial research ethics and conflicts of interest, medical device regulations, commonly used statistical methods, and related learning points and precautions. It is recommended that current and future researchers planning human trial projects actively participate, attend the full course and verify attendance for a total of 6 hours, plus an additional 2 hours for completing the assessment.

Related registration information is in the attachment.

https://forms.gle/eP5g8XxfdR4s1tx5A

 

IRB course registration

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