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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:
0920-0263
ICR Reference No:
201705-0920-008
Status:
Historical Active
Previous ICR Reference No:
201611-0920-007
Agency/Subagency:
HHS/CDC
Agency Tracking No:
0920-0263
Title:
Requirements for the Importation of Nonhuman Primates into the United States
Type of Information Collection:
Revision of a currently approved collection
Common Form ICR:
No
Type of Review Request:
Regular
OIRA Conclusion Action:
Approved with change
Conclusion Date:
08/15/2017
Retrieve Notice of Action (NOA)
Date Received in OIRA:
06/02/2017
Terms of Clearance:
Inventory as of this Action
Requested
Previously Approved
Expiration Date
08/31/2020
36 Months From Approved
09/30/2017
Responses
5,124
0
5,187
Time Burden (Hours)
921
0
943
Cost Burden (Dollars)
41,004
0
0
Abstract:
This information collection continues regulatory oversight of nonhuman primate importers through registration, reregistration, evaluation of standard operating procedures, receiving pre-shipment notification, reviewing requests for releasing shipments from CDC quarantine, and overseeing filovirus testing of nonhuman primates when required.
Authorizing Statute(s):
US Code:
42 USC 264
Name of Law: Regulations to Control Communicable Diseases
US Code:
19 USC 1411
Name of Law: Tariff Act of 1930 (As amended by the Safe Port Act of 2006)
EO: EO 13659 Name/Subject of EO: Streamlining the Export/Import Process for America's Businesses
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:
82 FR 12962
03/08/2017
30-day Notice:
Federal Register Citation:
Citation Date:
82 FR 25290
06/01/2017
Did the Agency receive public comments on this ICR?
Yes
Number of Information Collection (IC) in this ICR:
10
IC Title
Form No.
Form Name
Application for Importer Registration (Reregistration) - Nonhuman Primates
75.10A
Application for Registration as an Importer of Nonhuman Primates
Application for Registration as New Importer of Nonhuman Primates
75.10A
Application for Registration as an Importer of Nonhuman Primates
Documentation and Standard Operating Procedures - New Importer
Documentation and Standard Operating Procedures - Registered Importer
none
42 CFR 71.53
Filovirus Diagnostic Specimen Submission
Importer/Filer Documentation of Non-infectiousness
71.53
Documentation of Non-infectiousness
Importer/Filer of Nonhuman Primate Products
71.53
CDC Requested Data of Regulated Imports: Nonhuman Primate Products
Quarantine Release
Recordkeeping and Reporting Requirements for importing Nonhuman Primates
none
42 CFR 71.53
Recordkeeping and reporting Requirements for Importing Live Nonhuman Primates
75.1
CDC Requested Data on Regulated Imports - Live Nonhuman Primates
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
5,124
5,187
0
-63
0
0
Annual Time Burden (Hours)
921
943
0
-22
0
0
Annual Cost Burden (Dollars)
41,004
0
0
41,004
0
0
Burden increases because of Program Change due to Agency Discretion:
Yes
Burden Increase Due to:
Miscellaneous Actions
Burden decreases because of Program Change due to Agency Discretion:
Yes
Burden Reduction Due to:
Miscellaneous Actions
Short Statement:
This revision adjusts the burden based on the number of registered importers and the number of filovirus samples processed by CDC. A new IC separates new registrants from reregistrants.
Annual Cost to Federal Government:
$123,150
Does this IC contain surveys, censuses, or employ statistical methods?
No
Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002?
Yes
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?
Uncollected
Agency Contact:
Shari Steinberg 404 639-4942 sxw2@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:
06/02/2017
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