Well-Integrated Screening and Evaluation for Women Across the Nation (WISEWOMAN) Reporting System

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Form 0920-0612 Annual Progress Report	Form and Instruction	Modified	Available
0612 Att 6 MDE Submission Instructions Final.pdf	Supplementary Document	Uploaded 2019-05-10	Available
WISEWOMAN 1701 PIA 02-13-19.pdf	Supplementary Document	Uploaded 2019-05-10	Available
0612 Att 8 Consent to Participate in WISEWOMAN Prg Final.pdf	Supplementary Document	Uploaded 2019-05-10	Available
0612 Att 3 WISEWOMAN MDE Manual Final.pdf	Supplementary Document	Uploaded 2019-05-10	Available
0612 Att 2d 60-Day FRN Final.pdf	Supplementary Document	Uploaded 2019-05-10	Available
0612 Att 2b WISEWOMAN Prg Mgrs Directors & Data Mgrs Final.pdf	Supplementary Document	Uploaded 2019-05-10	Available
0612 Att 2a WISEWOMAN Awardees Final.pdf	Supplementary Document	Uploaded 2019-05-10	Available
0612 Att 1b PHSA Final.pdf	Supplementary Document	Uploaded 2019-05-10	Available
0612 Att 1a NBCCEDP Law Statute Final.pdf	Supplementary Document	Uploaded 2019-05-10	Available
OMB Change Request Summary 04.06.18.docx	Justification for No Material/Nonsubstantive Change	Uploaded 2018-04-11	Available
0612 SSB Final.docx	Supporting Statement B	Uploaded 2019-05-10	Available
0612 SSA Final iv tsl 051019.docx	Supporting Statement A	Uploaded 2019-05-10	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
37802	Well-Integrated Screening and Evaluation for Women Across the Nation (WISEWOMAN) Reporting System	Other-Screenshot	Modified
191867	Annual Progress Report	Form and Instruction	Modified

ICR Details

OMB Control No: 0920-0612	ICR Reference No: 201905-0920-005
Status: Historical Active	Previous ICR Reference No: 201804-0920-005
Agency/Subagency: HHS/CDC	Agency Tracking No: 0920-0612
Title: Well-Integrated Screening and Evaluation for Women Across the Nation (WISEWOMAN) Reporting System
Type of Information Collection: Reinstatement without change of a previously approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 08/14/2019
	Date Received in OIRA: 06/05/2019
Terms of Clearance:

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	08/31/2022	36 Months From Approved
Responses	63	0	0
Time Burden (Hours)	1,344	0	0
Cost Burden (Dollars)	0	0	0

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Abstract: CDC request OMB approval for a Reinstatement without change to the previously approved WISEWOMAN information collection. The data collected by the WISEWOMAN program are used to evaluate activities that are designed to improve public health practice, program performance, and assess program outcomes which are all aimed at reducing cardiovascular disease (CVD) risk factors among at-risk women and are the recipients of targeted interventions at the state, tribal, or local level funded by WISEWOMAN grants. The collection expiration date occurred before necessary approvals could be obtained.

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Authorizing Statute(s): PL: Pub.L. 101 - 354 300 Name of Law: The Breast and Cervical Cancer Mortality Prevention Act of 1990
   US Code: 42 USC 241 Name of Law: Public Health Service Act
  

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
	Not associated with rulemaking

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	83 FR 66269	12/26/2018
30-day Notice:	Federal Register Citation:	Citation Date:
	84 FR 26107	06/05/2019
Did the Agency receive public comments on this ICR? Yes

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Number of Information Collection (IC) in this ICR: 2

table that charts list of burden

IC Title	Form No.	Form Name
Well-Integrated Screening and Evaluation for Women Across the Nation (WISEWOMAN) Reporting System	0920-0612	WISEWOMAN Program MDE Manual Version 9.0 July 2013
Annual Progress Report	0920-0612	Annual Progress Report

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ICR Summary of Burden

table that charts list of burden

	Total Approved	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	63	0	0	63	0	0
Annual Time Burden (Hours)	1,344	0	0	1,344	0	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

Burden increases because of Program Change due to Agency Discretion: Yes

Burden Increase Due to: Miscellaneous Actions

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement: The burden has not changed.

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Annual Cost to Federal Government: $376,950

Does this IC contain surveys, censuses, or employ statistical methods? Yes Part B of Supporting Statement

Does this ICR request any personally identifiable information (see OMB Circular No. A-130 for an explanation of this term)? Please consult with your agency's privacy program when making this determination.     No

Does this ICR include a form that requires a Privacy Act Statement (see 5 U.S.C. §552a(e)(3))? Please consult with your agency's privacy program when making this determination.     No

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? No

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? No

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? No

Is this ICR related to the Pandemic Response? Uncollected

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Common Form ICR:  No

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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:

(a) It is necessary for the proper performance of agency functions;

(b) It avoids unnecessary duplication;

(c) It reduces burden on small entities;

(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;

(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;

(f) It indicates the retention periods for recordkeeping requirements;

(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:

(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;

(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.

(i) It uses effective and efficient statistical survey methodology (if applicable); and

(j) It makes appropriate use of information technology.

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.

Certification Date: 06/05/2019

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