Emergency Epidemic Investigation Data Collections - 3rd Quarter (April 1, 2020 - June 30, 2020)

ICR 202012-0920-006

OMB: 0920-1011

Federal Form Document

Forms and Documents
Document
Name
Status
Supplementary Document
2020-12-11
Supplementary Document
2020-12-11
Justification for No Material/Nonsubstantive Change
2020-12-11
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 202012-0920-006
Active 202012-0920-002
HHS/CDC 0920-1011-20RH
Emergency Epidemic Investigation Data Collections - 3rd Quarter (April 1, 2020 - June 30, 2020)
No material or nonsubstantive change to a currently approved collection   No
Regular
Approved without change 12/17/2020
Retrieve Notice of Action (NOA) 12/14/2020
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
805,759 0 947,000
402,874 0 473,500
0 0 0
This non-substantive change request is submitted to comply with the stated procedures in the approved EEI Generic ICR package (as specified in point 5 under Special Circumstances Relating to the Guidelines of 5 CFR 1320.5), “CDC maintains a library of data collection instruments that includes all final data collection instruments conducted under this generic ICR. This library and the updated burden numbers based on data collected via the “Burden Memo” are submitted to OMB quarterly as a non-substantive change to the generic ICR.” This non-substantive change request includes the following: Burden Memos (Appendix 1) and final data collection forms (Appendix 2) for the investigations conducted under 0920-1011 for which data collection was completed from April 1, 2020 to June 30, 2020.
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 805,759 947,000 0 -141,241 0 0
Annual Time Burden (Hours) 402,874 473,500 0 -70,626 0 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
No
Yes
Miscellaneous Actions
The actual burden for the one investigation completed during this quarter was 805,759 respondents and 402,874 burden hours. This is more than the 3,200 respondents and 1,600 burden hours that were projected in the GenIC requests for this investigation.
$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.
12/14/2020
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