WISEWOMAN Reporting System

Forms and Documents

Document Name	Status
Form 1 WISEWOMAN Reporting System Form and Instruction	Modified
Wisewoman IRB Approval Letter.pdf Supplementary Document	2006-11-15
WiseWoman Published 60d FRN.pdf Supplementary Document	2006-11-15
Public Comment and Response for Wisewoman 60-day FRN.doc Supplementary Document	2006-11-15
Public Comment and Response for Wisewoman 60-day FRN (2).doc Supplementary Document	2006-11-15
WiseWoman_Supp_Stmt_11-15-06 (A).doc Supporting Statement A	2006-11-15

IC Document Collections

IC ID	Document Title	Status
37802	WISEWOMAN Reporting System Form and Instruction	Modified

ICR Details

OMB Control No: 0920-0612	ICR Reference No: 200611-0920-004
Status: Historical Active	Previous ICR Reference No: 200605-0920-006
Agency/Subagency: HHS/CDC	Agency Tracking No:
Title: WISEWOMAN Reporting System
Type of Information Collection: Extension without change of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 01/09/2007
	Date Received in OIRA: 11/22/2006
Terms of Clearance:

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	01/31/2010	36 Months From Approved	01/31/2007
Responses	150	0	150
Time Burden (Hours)	2,160	0	2,160
Cost Burden (Dollars)	0	0	0

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Abstract: The Centers for Disease Control and Prevention is requesting an extension to continue to collect comprehensive cardiovascular disease screening and intervention services data collected by grantees funded through the Well-Integrated Screening and Evaluation for Women Across the National (WISEWOMAN) program. The purpose of the data collection is to evaluate the costs and effectiveness of the program.

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Authorizing Statute(s): PL: Pub.L. 101 - 354 300n-4a Name of Law: The Breast and Cervical Cancer Mortality Prevention Act of 1990
  

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:
	71 FR 57512	09/29/2006
30-day Notice:	Federal Register Citation:	Citation Date:
	71 FR 66530	11/15/2006
Did the Agency receive public comments on this ICR? Yes

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Number of Information Collection (IC) in this ICR: 1

IC Title	Form No.	Form Name
WISEWOMAN Reporting System	1	Wise woman Data User Manual

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ICR Summary 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	150	150	0	0	0	0
Annual Time Burden (Hours)	2,160	2,160	0	0	0	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

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

Burden Increase Due to:

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

Burden Reduction Due to:

Short Statement:

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Annual Cost to Federal Government: $360,000

Does this IC contain surveys, censuses, or employ statistical methods? No

Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002? No

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? Uncollected

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? Uncollected

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? Uncollected

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: 11/22/2006

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