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Federal forms, ICRs, and supporting documents

Information Collection Request

Emergency Epidemic Investigation Data Collections - Expedited Reviews (Y3Q4)

ICR 201911-0920-008 · OMB 0920-1011 · Historical Inactive

Forms and Documents
Document
Name
Status
Supporting Statement B
2019-11-20
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
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
2019-11-20
Supplementary Document
2013-11-20
Supporting Statement A
2019-12-10
IC Document Collections
IC ID
Document
Title
Status
ICR Details
0920-1011 201911-0920-008
Historical Inactive 201907-0920-001
HHS/CDC 0920-1011
Emergency Epidemic Investigation Data Collections - Expedited Reviews (Y3Q4)
Revision of a currently approved collection   No
Regular
Improperly submitted and continue 01/13/2020
Retrieve Notice of Action (NOA) 12/10/2019
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 36 Months From Approved 01/31/2020
36,000 0 36,000
18,000 0 18,000
0 0 0
The EEI Generic ICR is specifically designed to support CDC mission-critical functions by allowing CDC to deploy to the field to conduct Emergency Epidemic Investigations (EEIs) at the request of, and under the public health authority of, external partners seeking support for a rapid response to urgent public health problems. Data collection methods will vary depending on the circumstances and needs of the investigation and will include epidemiologic investigations, environmental assessment, and laboratory testing. The respondent universe is the population to which results will be generalized, and will vary depending on the outbreak or event, but is not a mechanism to collect data that can be generalized to the broader population. The population to which results are generalizable is limited to those potentially exposed to or affected by the health event under investigation.
US Code: 42 USC 301 Name of Law: PHSA
  
None
Not associated with rulemaking
  84 FR 46535 09/04/2019
84 FR 66908 12/05/2019
No
0
No
No
$1,586,352
Yes Part B of Supporting Statement
    No
    No
No
No
No
Uncollected
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.
12/10/2019