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Required00
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Document Submission Check List
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(PI Sign)
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0-1
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Exempt and Expedited Review Self-Assessment
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If applying for exempt or expedited review, this must be attached.
(PI Sign)
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Required.01
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New Protocol Review Application
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Please indicate version date.
(PI Sign)
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Required. 02
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Research Protocol
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Please indicate version date
(PI Sign)
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Required.03
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Informed Consent
□Use the committee template for the consent form (3-1)
□Use self-designed consent form: Please attach the consent form and the “Application for Exemption from Signing or Amendment to the Informed Consent Content” (3-2)
□Applying for exemption from research subjects signing/oral notice/webpage notice: Please attach the consent form content and the “Application for Exemption from Signing or Amendment to the Informed Consent Content” (3-2)
□Applying for full exemption from informed consent: Please attach the “Application for Exemption from Informed Consent” (3-3)
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Please indicate version date
- Please use the yyyy-mm-dd format to indicate the version date at the footer of each page.
- For self-designed, oral/webpage consent, the required information must follow Article 14 of the Human Subjects Research Act.
(PI Sign)
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04
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Research Tools
□Research Questionnaire
□Interview Outline
□Data Collection
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If applicable, please indicate version date.
(PI Sign)
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05
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Recruitment of research subjects advertisement materials
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If applicable, please indicate version date.
(PI Sign)
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06
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Relevant References by PI or others
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If applicable, please provide two articles from the last five years.
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Required.07
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CV and publication check list of the principal investigator, co-investigator, and sub-investigator.
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(PI Sign)
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Required. 08
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Proof of research ethics training (including principal investigator, co-investigator, sub-investigator, research assistants, graduate students, and all members involved in the research protocol)
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Please provide copies of research ethics training certificates from within the last 2 years, covering at least 6 hours of training.
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09
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Notification of Affiliated Institution Record (for externally commissioned protocols)
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Copies of documents proving the external PI has notified their affiliated institution’s research protocol management office.
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Required. 10
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Principal Investigator Agreement
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(PI Sign)
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11
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Other supplementary documents or relevant certifications
- If the research involves secondary data, please attach supplementary documents explaining the legality of the original data, such as certification of approval from other IRB/REC reviews.
- If instruments are used in the research, please attach safety or certification documents for the instruments.
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