NICHD Research Partner Satisfaction Surveys

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Form 1 survey	Form and Instruction	New	Available
Form 1 SIDS Summit Meetings	Form and Instruction	Unchanged	Available
Form 1 SIDS Summit Meetings	Form and Instruction	Unchanged	Available
Form 1 SIDS Summit Meetings	Form and Instruction	Unchanged	Available
Form 1 SIDS Summit Meetings	Form and Instruction	Unchanged	Available
Change Request for NICHD Generic Clearance 0925-0532 Memo[1].docx	Justification for No Material/Nonsubstantive Change	Uploaded 2010-10-01	Available
NICHD Research Partner Satisfaction Surveys-Section B..doc	Supporting Statement B	Uploaded 2007-10-16	Available
Renewal NICHD Suporting Statement-Final (7).doc	Supporting Statement A	Uploaded 2007-10-17	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
194799	Healthy Native Babies Post-training Survey	Form and Instruction	New	survey
182537	Web Based	Form and Instruction	Unchanged	SIDS Summit Meetings
182536	Telephone	Form and Instruction	Unchanged	SIDS Summit Meetings
182535	In-Person	Form and Instruction	Unchanged	SIDS Summit Meetings
182534	Paper Survey	Form and Instruction	Unchanged	SIDS Summit Meetings

ICR Details

OMB Control No: 0925-0532	ICR Reference No: 201010-0925-001
Status: Historical Active	Previous ICR Reference No: 200710-0925-003
Agency/Subagency: HHS/NIH	Agency Tracking No:
Title: NICHD Research Partner Satisfaction Surveys
Type of Information Collection: No material or nonsubstantive change to a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 10/01/2010
Retrieve Notice of Action (NOA)	Date Received in OIRA: 10/01/2010
Terms of Clearance: Previous terms of clearance apply: This generic ICR is approved on the understanding that the results obtained from any customer satisfaction surveys through this ICR will be used for internal agency purposes, as opposed to reports to Congress or formal program evaluations. This generic ICR is approved consistent with NIH agreement to submit individual collections to OMB prior to fielding, along with all necessary supporting statements (to include information about research design and analysis, incentives, burden estimates, approaches to address non-response bias, etc). OMB will aim to review each IC submission within 14 days; however, OMB approval should not be assumed if not explicitly granted, even if 14 days have elapsed since submission.

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	01/31/2011	01/31/2011	01/31/2011
Responses	28,000	0	28,000
Time Burden (Hours)	6,483	0	5,883
Cost Burden (Dollars)	0	0	0

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Abstract: This evaluation data collection is designed to improve the NICHD's program planning and management by obtaining direct feedback from NICHD research partners. These include researchers, clinicians, patients, and members of the public.

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Authorizing Statute(s): EO: EO 12862 Name/Subject of EO: SETTING CUSTOMER SERVICE STANDARDS
  

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:
	72 FR 40887	07/25/2007
30-day Notice:	Federal Register Citation:	Citation Date:
	72 FR 60380	10/24/2007
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 5

table that charts list of burden

IC Title	Form No.	Form Name
Healthy Native Babies Post-training Survey	1	survey
In-Person	1	SIDS Summit Meetings
Paper Survey	1	SIDS Summit Meetings
Telephone	1	SIDS Summit Meetings
Web Based	1	SIDS Summit Meetings

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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	28,000	28,000	0	0	0	0
Annual Time Burden (Hours)	6,483	5,883	0	600	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 Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) would like to request an additional 600 hours to our currently approved submission, Generic Clearance #0925-0532. At the time when the main submissions for generic clearances were submitted, I/Cs were created and therefore the burden was taken up without surveys attached to them. The process now is different and allows for sub-studies to be submitted without this problem.

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Annual Cost to Federal Government: $465,372

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

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]? No

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)? 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: 10/01/2010

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