View Information Collection Request (ICR) Package
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View Information Collection (IC) List
View Supporting Statement and Other Documents
Please note that the OMB number and expiration date may not have been determined when this Information Collection Request and associated Information Collection forms were submitted to OMB. The approved OMB number and expiration date may be found by clicking on the Notice of Action link below.
View Generic ICR - OIRA Conclusion
OMB Control No:
0920-1158
ICR Reference No:
201611-0920-005
Status:
Historical Active
Previous ICR Reference No:
Agency/Subagency:
HHS/CDC
Agency Tracking No:
16AOW
Title:
CDC I-Catalyst Program
Type of Information Collection:
New collection (Request for a new OMB Control Number)
Common Form ICR:
No
Type of Review Request:
Regular
OIRA Conclusion Action:
Approved with change
Conclusion Date:
01/23/2017
Retrieve Notice of Action (NOA)
Date Received in OIRA:
11/16/2016
Terms of Clearance:
Approved consistent with the understanding that collections submitted under this Generic will be conducted by CDC I-Catalyst project teams. These collections aim to solicit information from specific stakeholder groups that will collect qualitative outcomes intended to be utilized internally and not generalizable to broader populations. All substudies submitted under this OMB control number will include an abbreviated supporting statement part A (and Part B if necessary) and confirm that no incentives will be provided to responding participants.
Inventory as of this Action
Requested
Previously Approved
Expiration Date
01/31/2020
36 Months From Approved
Responses
3,000
0
0
Time Burden (Hours)
1,500
0
0
Cost Burden (Dollars)
87,480
0
0
Abstract:
I-Catalyst program is intended to help CDC employees develop ideas into solutions that address customer need and show value through a discovery, ideation, and prototyping process. Insights gathered from information collection will be gathered from informal, voluntary interviews and observations to assess how to best solve the problems of their customers rather than creating solutions that are not usable. Resulting data will be used for internal CDC decision making and to provide suggestions for improving development of public health solutions.
Authorizing Statute(s):
US Code:
42 USC 241
Name of Law: PHSA
Citations for New Statutory Requirements:
None
Associated Rulemaking Information
RIN:
Stage of Rulemaking:
Federal Register Citation:
Date:
Not associated with rulemaking
Federal Register Notices & Comments
60-day Notice:
Federal Register Citation:
Citation Date:
81 FR 38707
06/14/2016
30-day Notice:
Federal Register Citation:
Citation Date:
81 FR 80058
11/15/2016
Did the Agency receive public comments on this ICR?
Yes
Number of Information Collection (IC) in this ICR:
16
IC Title
Form No.
Form Name
Behavioral Health Data for Response Efforts: Interviews with Non-governmental Organizations (CSELS)
n/a
Interview Guide and Questions for Non-governmental Organizations
Behavioral Health Data for Response Efforts: Interviews with State, Tribal and Local Government Authorities (CSELS)
n/a
Behavioral Health Data for Response Efforts Interview Protocol Guide and Questions
Community-based Mosquito Surveillance - Maternal Child Health Providers [MHPs] (NCEZID)
n/a
Interview Guide for Material-Child Health Providers
Community-based Mosquito Surveillance - Pregnant Women (NCEZID)
n/a
Community-based Mosquito Surveillance – Pregnant Women Interview Guide and Questions
DSNS Communication Tool for Situational Awareness (OPHPR)
n/a
Interview Protocol Guide and Questions
Data Hub
Division of Global HIV and TB
HIV Guidelines (NCHHSTP)
n/a
Interview Guide
IIU Design Sprint
Influenza Surveillance (NCIRD)
n/a
NCIRD Influenza Surveillance Interview Protocol Guide and Questions
Occupational Safety Resources (NIOSH)
n/a
Occupational Safety Resources Interview Protocol Guide and Questions
Rapid Digitized Mapping (NCEZID)
n/a
NCEZID Rapid Digitized Mapping Interview Protocol Guide and Questions
Respiratory Protective Device Stockpiles
Sudden Infant Death and Investigation Report Form
Travelers Health - Travel Industry (NCEZID)
n/a
Travel Industry Interview Protocol Guide and Questions
Travelers Health with Travelers (NCEZID)
n/a
Interview Guide
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
3,000
0
0
3,000
0
0
Annual Time Burden (Hours)
1,500
0
0
1,500
0
0
Annual Cost Burden (Dollars)
87,480
0
0
87,480
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:
This is a new generic clearance request.
Annual Cost to Federal Government:
$123,000
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]?
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
Agency Contact:
Shari Steinberg 404 639-4942 sxw2@cdc.gov
Common Form ICR:
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:
(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:
11/16/2016
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