OMB
.report
Search
PHS Human Subjects and Clinical Trial Information (Part of RPPR, includes inclusion enrollment report)
PHS Research Performance Progress Report and Other Post-award Reporting (OD)
OMB: 0925-0002
IC ID: 225112
OMB.report
HHS/NIH
OMB 0925-0002
ICR 201701-0925-004
IC 225112
( )
⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0925-0002 can be found here:
2024-09-25 - Revision of a currently approved collection
2022-10-06 - Revision of a currently approved collection
Documents and Forms
Document Name
Document Type
Form 22
PHS Human Subjects and Clinical Trial Information (Part of RPPR, includes inclusion enrollment report)
Form
22 PHS Human Subjects and Clinical Trial Information - Land
Attachment 5B PHS Human Subjects and Clinical Trial Information - Landing Page.pdf
Form
23 PHS Human Subjects and Clinical Trial Information - Incl
Attachment 5B PHS Human Subjects and Clinical Trial Information - Inclusion Enrollment Report.pdf
Form
24 PHS Human Subjects and Clinical Trial Information - Sect
Attachment 5B PHS Human Subjects and Clinical Trial Information - Sections 1-5.pdf
Form
Information Collection (IC) Details
View Information Collection (IC)
IC Title:
PHS Human Subjects and Clinical Trial Information (Part of RPPR, includes inclusion enrollment report)
Agency IC Tracking Number:
Is this a Common Form?
No
IC Status:
New
Obligation to Respond:
Voluntary
CFR Citation:
Information Collection Instruments:
Document Type
Form No.
Form Name
Instrument File
URL
Available Electronically?
Can Be Submitted Electronically?
Electronic Capability
Form
22
PHS Human Subjects and Clinical Trial Information - Landing Page
Attachment 5B PHS Human Subjects and Clinical Trial Information - Landing Page.pdf
Yes
Yes
Fillable Fileable
Form
23
PHS Human Subjects and Clinical Trial Information - Inclusion Enrollment Report
Attachment 5B PHS Human Subjects and Clinical Trial Information - Inclusion Enrollment Report.pdf
Yes
Yes
Fillable Fileable
Form
24
PHS Human Subjects and Clinical Trial Information - Sections 1-5
Attachment 5B PHS Human Subjects and Clinical Trial Information - Sections 1-5.pdf
Yes
Yes
Fillable Fileable
Federal Enterprise Architecture Business Reference Module
Line of Business:
Health
Subfunction:
Public Health Monitoring
Privacy Act System of Records
Title:
FR Citation:
Number of Respondents:
6,420
Number of Respondents for Small Entity:
0
Affected Public:
Individuals or Households
Percentage of Respondents Reporting Electronically:
100 %
Approved
Program Change Due to New Statute
Program Change Due to Agency Discretion
Change Due to Adjustment in Agency Estimate
Change Due to Potential Violation of the PRA
Previously Approved
Annual Number of Responses for this IC
6,420
0
6,420
0
0
0
Annual IC Time Burden (Hours)
25,680
0
25,680
0
0
0
Annual IC Cost Burden (Dollars)
0
0
0
0
0
0
Documents for IC
Title
Document
Date Uploaded
No associated records found
Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.