PHS Research Performance Progress Report and Other Post-award Reporting (OD)

ICR 202207-0925-004

OMB: 0925-0002

Federal Form Document

Forms and Documents
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Supplementary Document
2022-07-27
Supplementary Document
2022-07-27
Supplementary Document
2022-07-27
Supplementary Document
2022-07-27
Supplementary Document
2022-07-27
Supplementary Document
2022-07-27
Supplementary Document
2022-07-27
Supplementary Document
2022-07-27
Justification for No Material/Nonsubstantive Change
2022-07-27
Supplementary Document
2021-08-11
Supporting Statement A
2021-08-11
Supplementary Document
2021-08-11
Supplementary Document
2021-08-11
Supplementary Document
2019-12-27
Supplementary Document
2017-01-25
Supplementary Document
2017-01-25
Supplementary Document
2017-01-25
ICR Details
0925-0002 202207-0925-004
Received in OIRA 202108-0925-002
HHS/NIH 20860
PHS Research Performance Progress Report and Other Post-award Reporting (OD)
No material or nonsubstantive change to a currently approved collection   No
Regular 07/27/2022
  Requested Previously Approved
09/30/2024 09/30/2024
411,699 411,699
532,249 532,249
0 0

The National Institutes of Health (NIH) and other Public Health Service (PHS) grantees are required to submit interim and final progress reports and other post-award documents associated with the monitoring, oversight, and closeout of an award. This 0925-0002 revision submission represents a collection of post-award reporting requirements previously collected under 0925-0002. Pre-award reporting requirements are simultaneously consolidated under 0925–0001 (expiration February 28, 2023) and the changes to the collection here are related. This collection is being revised to omit the Inclusion Enrollment Report form, which is being converted to a Common form to include the Department of Defense (DoD). The Inclusion Enrollment Report is used for all progress reporting involving NIH-defined clinical research. This form is used to report both planned and cumulative (or actual) enrollment, and describes the sex/gender, race, and ethnicity of the study participants. Starting in January 2022, NIH will require applicants and recipients to provide their Unique Entity Identifier (UEI) instead of the Data Universal Number System (DUNS) number. Also, the progress reporting forms will be updated to align with the Grants.gov updated Country and State lists.

US Code: 42 USC 288 Name of Law: National Research Act
  
None

Not associated with rulemaking

  86 FR 18994 04/12/2021
86 FR 43258 08/06/2021
No

18
IC Title Form No. Form Name
PHS 2271 10, 9 Post-Award eRA Commons Screen Shots ,   PHS 2271
PHS 2590 15, 11, 16, 14, 12, 15, 13 PHS 2590 Forms ,   Trainee Diversity Report ,   General Non-Fellowship Biographical Sketch Format Page ,   Fellowship Applicant Biographical Sketch Format Page ,   Fellowship Applicant Biographical Sketch Postdoctoral Sample ,   Fellowship Applicant Biographical Sketch Predoctoral Sample ,   Revised - Fellowship Applicant Biographical Sketch Format Page
iEdison 4, 5, 6, 7, 8 iEdison Burden Statement ,   iEdison Screen Shot Manage Utilization Report ,   iEdison screen shot Invention Disclosure Report ,   iEdison screen shot Patent Record ,   iEdison screen shot Registration Request Form
Biosketch (part of RPPR) 14, 13 General Non-Fellowship Biographical Sketch Format Page ,   Fellowship Applicant Biographical Sketch Format Page
Data Tables (Part of RPPR) 18 Introducation to the Data Tables
Data Tables (Part of Final RPPR) 13 Research Performance Progress Report (RPPR) and Final RPPR
Final RPPR - Core Data 13 Research Performance Progress Report (RPPR) and Final RPPR
PHS 3734 20 Attachment 18 PHS 374
PHS 416-7 28, 1 National Research Service Award Termination Notice ,   Post Award eRA Commons Screen Shots xTrain, xTRACT
PHS 568 3 HHS 568
PHS 6031-1 2 PHS 6031-1 FORMS-G
PHS Human Subjects and Clinical Trial Information (Part of Final RPPR, includes inclusion/enrollment) 23, 24, 22 PHS Human Subjects and Clinical Trial Information- Inclusion Enrollment Report ,   PHS Human Subjects and Clinical Trial Information Sections 1-6 ,   PHS Human Subjects and Clinical Trial Information Landing Page
PHS Human Subjects and Clinical Trial Information (Part of RPPR, includes inclusion enrollment report) 22, 24, 23 Landing Page ,   HSCT Sections 1-6 ,   Inclusion Enrollment Report
Publication Reporting 19 Attachment 11 MY BIB screenshot
RPPR Core Data 17 Research Performance Progress Report (RPPR) and Final RPPR Screenshots
SBIR/STTR Life Cycle Certification 28, 27 SBIR Life Cycle Certification ,   STTR Life Cycle Certification
Trainee Diversity Report (part of Final RPPR) 21 Trainee Diversity Report
Trainee Diversity Report (part of RPPR) 21 Attachment 7 Trainee Diversity Report

  Total Request Previously Approved Change Due to New Statute Change Due to Agency Discretion Change Due to Adjustment in Estimate Change Due to Potential Violation of the PRA
Annual Number of Responses 411,699 411,699 0 0 0 0
Annual Time Burden (Hours) 532,249 532,249 0 0 0 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
No
No
Changes made reflect an adjustment in burden hours. A decrease of 1,330 burden hours is due to the SBIR/STTR Final Progress Report no longer being accepted. Overall, the burden hour estimates for other PHS forms did not change.

$238,382
No
    Yes
    Yes
No
No
No
No
Mikia Currie 3014350941

  No

On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
 
 
 
 
 
 
 
    (i) Why the information is being collected;
    (ii) Use of information;
    (iii) Burden estimate;
    (iv) Nature of response (voluntary, required for a benefit, or mandatory);
    (v) Nature and extent of confidentiality; and
    (vi) Need to display currently valid OMB control number;
 
 
 
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.
07/27/2022


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