Emergency Epidemic Investigation Data Collections - Expedited Reviews (Y3Q4)

ICR 201902-0920-013

OMB: 0920-1011

Federal Form Document

Forms and Documents
Document
Name
Status
Form and Instruction
New
Form and Instruction
Unchanged
Form and Instruction
Unchanged
Form and Instruction
Unchanged
Form and Instruction
Unchanged
Supplementary Document
2019-02-22
Supplementary Document
2019-02-22
Justification for No Material/Nonsubstantive Change
2019-02-22
Justification for No Material/Nonsubstantive Change
2018-10-19
Justification for No Material/Nonsubstantive Change
2018-07-05
Supplementary Document
2018-04-11
Supplementary Document
2017-10-12
Supplementary Document
2017-07-10
Justification for No Material/Nonsubstantive Change
2017-06-07
Supplementary Document
2017-02-06
Supplementary Document
2017-02-06
Justification for No Material/Nonsubstantive Change
2017-02-06
Supporting Statement B
2016-10-13
Supplementary Document
2013-11-20
Supplementary Document
2013-11-20
Supplementary Document
2013-11-20
Supplementary Document
2013-11-20
Supplementary Document
2013-11-20
Supplementary Document
2013-11-20
Supplementary Document
2013-11-20
Supplementary Document
2016-10-13
Supplementary Document
2013-11-20
Supplementary Document
2016-10-13
Supplementary Document
2016-10-13
Supplementary Document
2016-10-13
Supplementary Document
2016-10-13
Supplementary Document
2013-11-20
Supporting Statement A
2016-10-13
ICR Details
0920-1011 201902-0920-013
Historical Active 201810-0920-007
HHS/CDC 0920-1011
Emergency Epidemic Investigation Data Collections - Expedited Reviews (Y3Q4)
No material or nonsubstantive change to a currently approved collection   No
Regular
Approved without change 03/29/2019
Retrieve Notice of Action (NOA) 03/14/2019
Previous terms continue: Approved consistent with the understanding that GenICs under this generic will be limited to acute public health emergencies resulting from outbreaks or events with undetermined agent, source, mode of transmission, or risk factors. Data collection for investigations conducted under this generic will not exceed 90 days. Investigations conducted for the primary purpose of program evaluation, surveillance, needs assessment, or research (e.g., to contribute to generalizable knowledge) are excluded from this generic pathway.
  Inventory as of this Action Requested Previously Approved
01/31/2020 01/31/2020 01/31/2020
36,000 0 36,000
18,000 0 18,000
0 0 0

This Generic ICR allows CDC to responsd to external partner requests for assistance during outbreaks or other urgent events, EEI data collections aim to identify the agents, sources, modes of transmission, or risk factors to effectively implement rapid prevention and control measures. This request is the quarterly report of inventory for 01OCT2018 - 31DEC2018.

US Code: 42 USC 301 Name of Law: PHSA
  
None

Not associated with rulemaking

  81 FR 46675 07/18/2016
81 FR 66028 09/26/2016
No

  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 36,000 36,000 0 -124 124 0
Annual Time Burden (Hours) 18,000 18,000 0 -41 41 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
No
Yes
Miscellaneous Actions
Non-Substantive Change Request is being submitted to comply with the stated procedures in the approved EEI Generic ICR package to reflect the actual burden for the two investigations completed during this quarter was 124 respondents and 41 burden hours.

$1,547,376
Yes Part B of Supporting Statement
    No
    No
No
No
No
Uncollected
Jeffrey Zirger 404 639-7118 [email protected]

  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:
 
 
 
 
 
 
 
    (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;
 
 
 
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.
03/14/2019


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