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:
0920-0134
ICR Reference No:
201611-0920-006
Status:
Historical Active
Previous ICR Reference No:
201608-0920-009
Agency/Subagency:
HHS/CDC
Agency Tracking No:
17EQ
Title:
Foreign Quarantine Regulations (42CFR71)
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:
11/17/2016
Retrieve Notice of Action (NOA)
Date Received in OIRA:
11/16/2016
Terms of Clearance:
Inventory as of this Action
Requested
Previously Approved
Expiration Date
05/31/2019
05/31/2019
05/31/2019
Responses
363,228
0
363,228
Time Burden (Hours)
82,779
0
82,779
Cost Burden (Dollars)
5,292
0
5,292
Abstract:
Request to change the method for respondents to submit forms; forms can be submitted via the International Trade Data System and the Automated Cargo Environment. No change to burden or forms.
Authorizing Statute(s):
Statute at Large:
42 Stat. 71
US Code:
42 USC 264
Name of Law: Public Health Service 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:
80 FR 34645
06/17/2015
30-day Notice:
Federal Register Citation:
Citation Date:
80 FR 59779
10/02/2015
Did the Agency receive public comments on this ICR?
No
Number of Information Collection (IC) in this ICR:
19
IC Title
Form No.
Form Name
42CFR71.21(c) Recordkeeping--Medical Logs
42CFR71.32(b)_Importer Documentation of Non Infectiousness (no form)
42CFR71.33(c) Report by Persons in Isolation or Surveillance ((no form))
42CFR71.35_Report of Dealth Illness During Stay in Port ((verbal, no form))
42CFR71.51(b)(3) Importer Dogs/Cats: Record of Sickness or Deaths ((verbal, no form))
42CFR71.51(c )(1)(d)_Valid Rabies Vacinnation Certificates ((verbal, no form))
42CFR71.51(c)(i)(ii)&(iii)_Exemption Criteria for the Importation of a Dog
42CFR71.52(d)_Turtle Importation Permits ((verbal, no form))
42CFR71.55 & 71.32_Dead Bodies--Death Certificates
42CFR71.56(a)(2)_African Rodents--Request for Exemption
42CFR71.56(a)(iii)_Appeal (Importer)
Att D_71.51(c)(2)_NOTICE TO OWNERS AND IMPORTERS OF DOGS: Requirement for Dog Confinement
CDC Form 75.37 (f.4.421)
NOTICE TO OWNERS AND IMPORTERS OF DOGS: Requirement for Dog Confinement
Att E_Application for Permission to Import A Dog Inadequately Immunized Against Rabies
CDC Form 71.51(c )(2)(d), CDC Form 71.51(c)(2)(d) rev082016
Application for Permission to Import a Dog Inadequately Immunized Against Rabies
,
Application for a Permit to Import A Dog Inadequately Immunized Against Rabies
Att H_42CFR71.21(a )_ Maritime Conveyance Illness or Death Investigation Form
42CFR 71.21(a), None
Maritime Conveyance Illness or Death Investigation Form
,
Cumulative Influenza/Influenza-Like Illness (ILI) Form
Att I_42CFR71.21(b)_Death/Illness Reports from Aircraft
Att J_42CFR71.21(c )_(MIDRS) Gastrointestinal Illness Report
42CFR71.21(c )
(MIDRS) Gastrointestinal Illness Report
Att K & L_42CFR 71.51_CDC Requested Data on Regulated Imports: Domestic Dogs & Cats
PGA-1, PGA-3
CDC Requested Data on Regulated Imports: Domestic Dogs(42CFR 71.51)
,
CDC Requested Data on Regulated Imports: Domestic Cats (42CFR71.51)
Att M_42CFR71.56_CDC Requested Data on Regulated Imports: Live African Rodents (PGA Message Set)
42CFR71.56
CDC Requested Data on Regulated Imports: Live African Rodents
Att N _CDC Requested Data on Regulated Imports: Products of African Rodents (42CFR71.56); Products of All Family Viverridae (42CFR71.32)
PGA-1
CDC Requested Data on Regulated Imports: Products of African Rodents (42CFR71.56); Products of All Family Viverridae (42CFR71.32)
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
363,228
363,228
0
0
0
0
Annual Time Burden (Hours)
82,779
82,779
0
0
0
0
Annual Cost Burden (Dollars)
5,292
5,292
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:
$638,622
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?
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:
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:
11/16/2016
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