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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 ICR - OIRA Conclusion
OMB Control No:
0920-0199
ICR Reference No:
202206-0920-007
Status:
Active
Previous ICR Reference No:
202101-0920-009
Agency/Subagency:
HHS/CDC
Agency Tracking No:
0920-0199
Title:
Import Permit Applications (42 CFR 71.54)
Type of Information Collection:
No material or nonsubstantive change to a currently approved collection
Common Form ICR:
No
Type of Review Request:
Regular
OIRA Conclusion Action:
Approved without change
Conclusion Date:
06/28/2022
Retrieve Notice of Action (NOA)
Date Received in OIRA:
06/13/2022
Terms of Clearance:
Inventory as of this Action
Requested
Previously Approved
Expiration Date
08/31/2024
08/31/2024
08/31/2024
Responses
2,483
0
2,483
Time Burden (Hours)
764
0
764
Cost Burden (Dollars)
29,228
0
29,228
Abstract:
This information collection supports Section 361 of the Public Health Service (PHS) Act (42 U.S.C. 264) and prevents the introduction, transmission, or spread of communicable diseases from foreign countries into the States or possessions, or from one State or possession into any other State or possession. This is a request for nonmaterial/non-substantive changes to reflect the changes in the published 6th edition of Biosafety in Microbiological and Biomedical Laboratories (BMBL) and will not affect the burden in completing the form.
Authorizing Statute(s):
US Code:
42 USC CFR Part 71.55
Name of Law: Importation of Human Remains
US Code:
42 USC 264
Name of Law: PHSA
US Code:
42 USC CFR Part 71.54
Name of Law: FOREIGN QUARANTINE - Subpart F--Importations
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:
85 FR 66987
10/21/2020
30-day Notice:
Federal Register Citation:
Citation Date:
86 FR 14120
03/12/2021
Did the Agency receive public comments on this ICR?
Yes
Number of Information Collection (IC) in this ICR:
4
IC Title
Form No.
Form Name
Application for Permit to Import Infectious Biological Agents into the United States
n/a
Application for Permit to Import Infectious Biological Agents into the United States
Application for Permit to Import Infectious Biological Agents into the United States-SUBSEQUENT TRANSFERS
n/a
Application for Permit to Import Infectious Biological Agents into the United States
Application for Permit to Import Infectious Human Remains into the United States
n/a
Application for Permit to Import Infectious Human Remains into the United States
Application for Permit to Import or Transport Live Bats (71.54)
n/a
Application for Permit to Import or Transfer Live Bats
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
2,483
2,483
0
0
0
0
Annual Time Burden (Hours)
764
764
0
0
0
0
Annual Cost Burden (Dollars)
29,228
29,228
0
0
0
0
Burden increases because of Program Change due to Agency Discretion:
No
Burden Increase Due to:
Burden decreases because of Program Change due to Agency Discretion:
No
Burden Reduction Due to:
Short Statement:
The Import Permit Program implemented a new electronic data collection system that is more efficient and reduces the need to consult guidance documents. There is also an adjustment to the estimated number of respondents requesting permits to import live bats.
Annual Cost to Federal Government:
$1,335,495
Does this IC contain surveys, censuses, or employ statistical methods?
Yes
Part B of Supporting Statement
Does this ICR request any personally identifiable information (see
OMB Circular No. A-130
for an explanation of this term)? Please consult with your agency's privacy program when making this determination.
No
Does this ICR include a form that requires a Privacy Act Statement (see
5 U.S.C. §552a(e)(3)
)? Please consult with your agency's privacy program when making this determination.
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?
No
Agency Contact:
Kevin Joyce 404 639-1944 kdj7@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:
06/13/2022
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