OMB.report

Federal forms, ICRs, and supporting documents

Information Collection Request

Virus-Serum-Toxin Act and Regulations in 9 CFR Subchapter, Parts 101-124

ICR 201307-0579-010 · OMB 0579-0013 · Historical Active

Forms and Documents
DocumentTypeStatusAvailability
Form APHIS 2001 Virus-Serum-Toxin Act and Regulations - Business Form Modified Available
2013 SS 0013a.docx Supporting Statement A Uploaded 2013-08-26 Available
2013 APHIS 79 - 0013v1.xlsx Supplementary Document Uploaded 2013-08-22 Repair queued
2013 APHIS 71v2 - 0013.xlsx Supplementary Document Uploaded 2013-08-26 Repair queued
IC Document Collections
IC IDCollectionTypeStatusForm
2084 Virus-Serum-Toxin Act and Regulations - Business Form Modified
200319 Virus-Serum-Toxin Act and Regulations - Individual Unchanged
183917 Virus-Serum-Toxin Act and Regulations - State Unchanged
ICR Details
0579-0013 201307-0579-010
Historical Active 201110-0579-002
USDA/APHIS
Virus-Serum-Toxin Act and Regulations in 9 CFR Subchapter, Parts 101-124
Revision of a currently approved collection   No
Regular
Approved without change 10/23/2013
Retrieve Notice of Action (NOA) 08/26/2013
Previous terms of clearance remain in effect.
  Inventory as of this Action Requested Previously Approved
10/31/2014 36 Months From Approved 10/31/2013
39,670 0 19,304
78,382 0 74,386
0 0 0
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).
US Code: 21 USC 151-159 Name of Law: VIRUS-SERUM-TOXIN ACT
  
None
Not associated with rulemaking
  78 FR 103 05/29/2013
78 FR 161 08/20/2013
Yes
3
IC Title Form No. Form Name
Virus-Serum-Toxin Act and Regulations - Individual
Virus-Serum-Toxin Act and Regulations - Business APHIS 2020, APHIS 2070, APHIS 2072, APHIS 2071, APHIS 2046, APHIS 2018, APHIS 2047, APHIS 2046S (spanish), APHIS 2005, APHIS 2001, APHIS 2008, APHIS 2008A, APHIS 2047S (Spanish), APHIS 2003, APHIS 2007, APHIS 2015, APHIS 2017 APPLICATION FOR US VETERINARY BIOLOGICS ESTABLISHMENT LICENSE ,   APPLICATION FOR US VETERINARY BIOLOGICAL PRODUCT LICENSE ,   CONTACT AND QUALIFICATIONS OF VETERINARY BIOLOGICS PERSONNEL ,   TRANSMITTAL OF LABLES AND CIRCULARS OR OUTLINES ,   OFFICIAL EXPORT CERTIFICATE FOR ANIMAL BIOLOGICAL PRODUCTS ,   REQUEST FOR REFERENCE, REAGENT, OR REAGENT SEED MATERIAL ,   APPLICATION FOR UNITED STATES VETERINARY BIOLOGICAL PRODUCT PERMIT ,   AHIPMENT AND RECEIPT OF BIOLOGICS SAMPLES ,   VETERINARY BIOLOGICS PRODUCTION AND TEST REPORT ,   CONTINUATION FOR VETERINARY BIOLOGICS PRODUCTION AND TEST REPORT ,   CERTIFICATE OF LICENSING AND INSPECTION ,   CERTIFICADO DE LICENCIA E INSPECCION ,   CERTIFICATE OF LICENSING AND INSPECTION ,   CERTIFICADO DE LICENCIA E INSPECTION ,   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 Confirmation Testing by APHIS
Virus-Serum-Toxin Act and Regulations - State
  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 39,670 19,304 0 90 20,276 0
Annual Time Burden (Hours) 78,382 74,386 0 128 3,868 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
Yes
Miscellaneous Actions
No
APHIS' 2013 burden calculation imposed by this collection increased by 18 respondents, from 202 to 220. Total responses increased by 20,366, from 19,304 to 39,670 and total burden hours increased by 3,996, from 74,386 in 2011 to 78,382 total burden hours in 2013. These changes are do to adjustments and program changes in the forms and regulations.
$1,316,149
No
No
No
No
No
Uncollected
Donna Malloy 301 734-3277
  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:
 
 
 
 
 
 
 
    (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;
 
 
 
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.
08/26/2013