View Information Collection Request (ICR) Package
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COMMENT
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OMB Control No:
0579-0127
ICR Reference No:
202604-0579-002
Status:
Received in OIRA
Previous ICR Reference No:
202404-0579-001
Agency/Subagency:
USDA/APHIS
Agency Tracking No:
0579-0127
Title:
9 CFR 75 Communicable Diseases in Horses
Type of Information Collection:
Revision of a currently approved collection
Common Form ICR:
No
Type of Review Request:
Regular
Date Submitted to OIRA:
05/12/2026
Requested
Previously Approved
Expiration Date
36 Months From Approved
06/30/2026
Responses
1,156,816
1,156,728
Time Burden (Hours)
96,225
92,610
Cost Burden (Dollars)
0
0
Abstract:
The purpose of this collection is to ensure the safe movement of horses through the use of several forms certifying their well being, and to report activities involved in approving laboratories to conduct testing for equine infectious anemia.
Authorizing Statute(s):
US Code:
21 USC 117
Name of Law: Animal Industry Act of 1884
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:
91 FR 1739
01/15/2026
30-day Notice:
Federal Register Citation:
Citation Date:
91 FR 25523
05/11/2026
Did the Agency receive public comments on this ICR?
Yes
Number of Information Collection (IC) in this ICR:
2
IC Title
Form No.
Form Name
Communicable Diseases in Horses - Private sector
VS 10-15, VS 10-16, VS 10-11
Agreement to Conduct Equine Infectious Anemia (EIA) Testing
,
Application to Conduct Laboratory Equine Infectious Anemia (EIA) Testing
,
Equine Infectious Anemia Laboratory Test
Communicable Diseases in Horses - State
VS 10-16
Application to Conduct Laboratory Equine Infectious Anemia (EIA) Testing
ICR Summary of Burden
Total Request
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
1,156,816
1,156,728
0
-3
91
0
Annual Time Burden (Hours)
96,225
92,610
0
-1
3,616
0
Annual Cost Burden (Dollars)
0
0
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:
Yes
Burden Reduction Due to:
Miscellaneous Actions
Short Statement:
APHIS is seeking approval of a revision of a currently approved information collection request. The currently approved ICR is for 235,018 respondents, 1,156,728 total annual responses, and 92,610 total annual burden hours. This request is for 235,015 respondents, 1,156,816 estimated total responses and 96,225 estimated burden hours. There are no third-party disclosure burden estimates hours. Change(s) in estimate due to Agency discretion include: There is a program change decrease of -3 responses and -1 total burden hours. • Item 1: Removal of the VS Form 1-27 from this collection, resulting in 3 fewer responses and 1 less burden hour. This form has been moved to the new VS Permit information collection. Change(s) in estimate due to adjustments in estimate include: There is an adjustment decrease of -3 respondents, however; there is an increase of +91 responses and +3,615 total burden hours. • Item 1: Adjusting the number of responses to the investigation information collection (formerly VS 10-12) from 15 to 100, the number of respondents from 3 to 40, and the number of burden hours from 8 to 150. This is due to an increase in the number of inspections owing to an increase in a type of illicit racing called “bushtrack” racing, often supported by illegal animal movements. This activity can involve EIA-exposed animals which in turn expose other equines, spreading the disease. • Item 2: Adjusting the number of respondents for the agreement to approve livestock facilities from 4 to 10, the number of responses from 4 to 10, and the number burden hours from one to five. The program added several approved facilities to the overall number since the previous renewal, and corrected the time needed to review and approve accordingly (doubling the previous estimate from .25 to .5). • Item 3: The program adjusted the amount of time needed to review requirements and interview laboratory personnel from half an hour to 2 hours to more accurately reflect the process, resulting in an increase of burden hours from 5 to 20. Time corrections were based on consultation with the experts named in the answer to Question 8, who wanted to ensure APHIS accounted for the time needed for follow up questions and other time contributors. • Item 4: Adjusted the response time for completing the VS 1-11 to represent what is posted on the form from .08 to .083 has added 455 total annual burden hours.
Annual Cost to Federal Government:
$10,811,876
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.
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:
Lisa Rochette 919 855-7276
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:
05/12/2026
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