Emergency Epidemic Investigation Data Collections - Increase in Respondents

ICR 202012-0920-002

OMB: 0920-1011

Federal Form Document

Forms and Documents
Document
Name
Status
Justification for No Material/Nonsubstantive Change
2020-12-04
Justification for No Material/Nonsubstantive Change
2020-09-01
Supplementary Document
2020-04-15
Supplementary Document
2020-04-07
Justification for No Material/Nonsubstantive Change
2020-04-07
Supplementary Document
2020-02-12
Justification for No Material/Nonsubstantive Change
2020-02-12
Supporting Statement A
2020-01-15
Supporting Statement B
2020-01-15
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
2019-11-20
Supplementary Document
2013-11-20
Supplementary Document
2016-10-13
Supplementary Document
2019-11-20
Supplementary Document
2016-10-13
Supplementary Document
2020-01-15
Supplementary Document
2013-11-20
IC Document Collections
IC ID
Document
Title
Status
ICR Details
0920-1011 202012-0920-002
Historical Active 202009-0920-002
HHS/CDC 0920-1011-20RT/2
Emergency Epidemic Investigation Data Collections - Increase in Respondents
No material or nonsubstantive change to a currently approved collection   No
Regular
Approved without change 12/10/2020
Retrieve Notice of Action (NOA) 12/04/2020
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
01/31/2023 01/31/2023 01/31/2023
947,000 0 36,000
473,500 0 473,500
0 0 0
The purpose of this non-substantive change request is for OMB approval for an increase in the number of respondents for this EEI generic ICR, which is necessary to ensure CDC’s ability to respond to the COVID-19 pandemic.
US Code: 42 USC 301 Name of Law: PHSA
  
None
Not associated with rulemaking
  84 FR 46535 09/04/2019
84 FR 66908 12/06/2019
No
0
  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 947,000 36,000 0 911,000 0 0
Annual Time Burden (Hours) 473,500 473,500 0 0 0 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
No
No
$1,586,352
Yes Part B of Supporting Statement
    No
    No
No
No
No
Yes
Thelma Sims 4046394771
  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.
12/04/2020
© 2024 OMB.report | Privacy Policy