View Information Collection Request (ICR) Package
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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:
0579-0013
ICR Reference No:
201905-0579-005
Status:
Historical Active
Previous ICR Reference No:
201804-0579-004
Agency/Subagency:
USDA/APHIS
Agency Tracking No:
Title:
Virus-Serum-Toxin Act and Regulations in 9 CFR Subchapter, Parts 101-124
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:
05/29/2019
Retrieve Notice of Action (NOA)
Date Received in OIRA:
05/20/2019
Terms of Clearance:
Inventory as of this Action
Requested
Previously Approved
Expiration Date
02/28/2022
02/28/2022
02/28/2022
Responses
298,820,801
0
298,820,801
Time Burden (Hours)
122,998
0
122,998
Cost Burden (Dollars)
0
0
0
Abstract:
The purpose of this collection is to verify that compliance requirements for biological products used in the United States are met (i.e., the products are pure, safe, potent, and effective).
Authorizing Statute(s):
US Code:
21 USC 151-159
Name of Law: VIRUS-SERUM-TOXIN ACT
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:
83 FR 4024
01/29/2018
30-day Notice:
Federal Register Citation:
Citation Date:
83 FR 47874
09/21/2018
Did the Agency receive public comments on this ICR?
No
Number of Information Collection (IC) in this ICR:
4
IC Title
Form No.
Form Name
Virus-Serum-Toxin Act and Regulations - Business
APHIS Form 2080, APHIS Form 2018, APHIS Form 2003, APHIS Form 2005, APHIS Form 2008, APHIS Form 2008A, APHIS Form 2047S, APHIS Form 2048, APHIS Form 2072, APHIS Form 2081, APHIS Form 2009, APHIS Form 2015, APHIS Form 2017, APHIS Form 2001, APHIS Form 2046S, APHIS Form 2070, APHIS Form 2071, APHIS Form 2007, APHIS Form 2020, APHIS Form 2046, APHIS Form 2047, APHIS Form 2049
Application for United States Veterinary Biologics Establishment License
,
Application for United States Veterinary Biological Product License
,
Application for United States Veterinary Biological Product Permit
,
Contact and Qualifications of Veterinary Biologics Personnel
,
Veterinary Biologics Production and Test Report
,
Continuation for Veterinary Biologics Production and Test Report
,
Center for Veterinary Biologics Inspection and Compliance Facility Document Submission Worksheet
,
Transmittal of Labeling or Outlines
,
Official Export Certificate for Animal Biological Products
,
Shipment and Receipt of Biologics Samples
,
Certificate of Licensing and Inspection (Unrestricted)
,
Certificate of Licensing and Inspection (Unrestricted) (Spanish)
,
Certificate of Licensing and Inspection (Restricted)
,
Certificate of Licensing and Inspection (Restricted) (Spanish)
,
Center for Veterinary Biologics Inspection and Compliance E-Submission Form
,
Veterinary Biologics Regulatory E-Submission Form Policy, Evaluation, and Licensing
,
Application for Authorization to Ship Master Seed or Cell Samples for Confirmatory Testing by APHIS
,
Application for Authorization to Ship Experimental Veterinary Biological Products
,
Application for Authorization to Ship Biological Product Samples for Confirmatory Testing by APHIS
,
Adverse Event Report Follow-Up Information
,
Request for Reference, Reagent, or Reagent Seed Material
,
Adverse Event Report
Virus-Serum-Toxin Act and Regulations - Foreign Gov't
Virus-Serum-Toxin Act and Regulations - Individual
APHIS Form 2080, APHIS Form 2081
Adverse Event Report Follow-Up Information
,
Adverse Event Report
Virus-Serum-Toxin Act and Regulations - State
APHIS Form 2080, APHIS Form 2081
Adverse Event Report Follow-Up Information
,
Adverse Event Report
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
298,820,801
298,820,801
0
0
0
0
Annual Time Burden (Hours)
122,998
122,998
0
0
0
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:
No
Burden Reduction Due to:
Short Statement:
Annual Cost to Federal Government:
$1,932,946
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?
Uncollected
Agency Contact:
Donna Malloy 301 734-3277
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:
05/20/2019
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