Request for Generic Clearance to Conduct Voluntary Customer/Partner Surveys

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Form 1 NLM Gateway Website Mobile User Survey	Form and Instruction	New	Available
Form 1 User Satisfaction Survey for MICAD	Form	New	Available
Form 1 PubChem Users	Form	New	Available
Form 1 User Satisfaction Survey for Principal Investigators of Other Screening/Probe Production Centers	Form and Instruction	New	Available
Form 1 Scientific Meetings and Non-Users of the Molecular Libraries Screening/Probes Production	Form and Instruction	New	Available
Form 1 Survey for Compound Providers of the Molecular Libraries Screening/Production Centers Network	Form and Instruction	New	Available
Form 1 Assay Providers of the Molecular Libraries	Form and Instruction	New	Available
OMB Memo Nonsubstantive Change 0476.doc	Justification for No Material/Nonsubstantive Change	Uploaded 2008-10-10	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
189060	NLM Gateway Website Mobile User Survey	Form and Instruction	New
188924	User Satisfaction Survey for MICAD	Form	New
188366	PubChem Users	Form	New
188070	User Satisfaction Survey for Principal Investigators of Other Screening/Probe Production Centers	Form and Instruction	New
187570	Scientific Meetings and Non-Users of the Molecular Libraries Screening/Probes Production	Form and Instruction	New
187241	Survey for Compound Providers of the Molecular Libraries Screening/Production Centers Network	Form and Instruction	New
187034	Assay Providers of the Molecular Libraries	Form and Instruction	New

ICR Details

OMB Control No: 0925-0476	ICR Reference No: 200810-0925-004
Status: Historical Active	Previous ICR Reference No: 200607-0925-010
Agency/Subagency: HHS/NIH	Agency Tracking No:
Title: Request for Generic Clearance to Conduct Voluntary Customer/Partner 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: 10/27/2008
	Date Received in OIRA: 10/14/2008
Terms of Clearance: NIH should submit each survey as a generic IC. Along with each IC, NIH should include a memo describing the study goal, study design, sample characteristics and size and any incentives to be used.

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	07/31/2009	07/31/2009	07/31/2009
Responses	19,758	0	19,758
Time Burden (Hours)	2,680	0	2,680
Cost Burden (Dollars)	0	0	0

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Abstract: Executive Order 12862 directs Federal Agencies to survey customers to determine the kind and quality of services they want. NLM is requesting extension of OMB approval for generic clearance to conduct a number of customer/partner satisfaction surveys. NLM will collect and use information gathered through customer and/or partner surveys to identify strengths and weaknesses in current service provisions and to make improvements that are practical and feasible.

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Authorizing Statute(s): None

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

Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 7

table that charts list of burden

IC Title	Form No.	Form Name
User Satisfaction Survey for Principal Investigators of Other Screening/Probe Production Centers	1, 2	survey ,   revised survey
PubChem Users	1	survey
Scientific Meetings and Non-Users of the Molecular Libraries Screening/Probes Production	1	survey
NLM Gateway Website Mobile User Survey	1	survey
Assay Providers of the Molecular Libraries	1	survey
Survey for Compound Providers of the Molecular Libraries Screening/Production Centers Network	1	Survey
User Satisfaction Survey for MICAD	1	survey

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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	19,758	19,758	0	0	0	0
Annual Time Burden (Hours)	2,680	2,680	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: $0

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]? 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: 10/14/2008

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