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人體研究倫理審查委員會
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SOPs
SOPs
Cited (10)
2021/12/29 15:44:23
2771
Personal Management
01.
The Organizational Charter of the First/Second IRB Committees
02.
The Organizational Chart of the First/Second IRB Committees
03.
Responsibilities of IRB Members and Staff
Regulations of Operation
04.
SOP for Education and Training of the First/Second IRB Committees
05.
SOP for Confidentiality and Conflict of Interest Statement
06.
SOP for Review by Expert Consultants
07.
SOP of Managing Protocol Submissions
08.
SOP for New Protocol Review
09.
SOP for Exempt Review
10.
SOP for Expedited Review
11.
SOP for Full Board Review
12.
SOP for Data and Safety Monitoring Plan
13.
SOP for Protocol Amendments
14.
SOP for Continuing Review
15.
SOP for Adverse Drug Reaction, Serious Adverse Event or Unanticipated Problem Monitoring
16.
SOP for Protocol Deviation/Violation
17.
SOP for Monitoring Visits
18.
SOP for Study Closure
19.
SOP for Handling Subject Complaints
20.
SOP for Protocol Suspension or Termination
21.
SOP for Handling Conflict of Interest in Clinical Study
22.
SOP for IRB Board Meetings
23.
SOP for Extraordinary IRB Meetings
24.
SOP for Management in Multicenter Studies
25.
SOP for Reviewing Non-TCVGH Research Protocols
26.
Sop for Document Management
27.
SOP for Creating and Updating Standardized Documents
28.
SOP for Definitions
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