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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:
202007-0920-010
Status:
Historical Active
Previous ICR Reference No:
201705-0920-008
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 without change
Conclusion Date:
09/28/2020
Retrieve Notice of Action (NOA)
Date Received in OIRA:
08/14/2020
Terms of Clearance:
Inventory as of this Action
Requested
Previously Approved
Expiration Date
09/30/2023
36 Months From Approved
09/30/2020
Responses
651
0
5,124
Time Burden (Hours)
184
0
921
Cost Burden (Dollars)
8,772
0
41,004
Abstract:
The goal of this information collection is to continue 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
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:
84 FR 66899
12/06/2019
30-day Notice:
Federal Register Citation:
Citation Date:
85 FR 49373
08/13/2020
Did the Agency receive public comments on this ICR?
Yes
Number of Information Collection (IC) in this ICR:
9
IC Title
Form No.
Form Name
Application for Importer Registration (Re-registration) - Nonhuman Primates
CDC 75.10
Application for Registration as an Importer of Nonhuman Primates
Application for Registration as New Importer of Nonhuman Primates
CDC 75.10
Application for Registration as an Importer of Nonhuman Primates
Documentation and Standard Operating Procedures - New Importer
Documentation and Standard Operating Procedures - Registered Importer
Filovirus Diagnostic Specimen Submission
n/a
Ebola Diagnostic Specimen Submission Form for quarantined non-human primates
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: Notification of shipment arrival
Recordkeeping and reporting Requirements for Importing Live Nonhuman Primates
75.1
CDC Requested Data on Regulated Imports - Live Nonhuman Primates
Statements regarding the health of the nonhuman primates during travel and CDC quarantine
Statements, including necropsy reports, about the nonhuman primates upon their release from CDC quarantine
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
651
5,124
0
-4,473
0
0
Annual Time Burden (Hours)
184
921
0
-737
0
0
Annual Cost Burden (Dollars)
8,772
41,004
0
-32,232
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:
Based on the number of registered importers and number of filovirus samples processed by CDC, CDC is adjusting downward the number of burden hours for four of the information collections.
Annual Cost to Federal Government:
$136,267
Does this IC contain surveys, censuses, or employ statistical methods?
No
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.
Yes
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:
Renita Macaluso 770 488-6458 arp5@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:
08/14/2020
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