Restrictions on Interstate Travel of Persons

Forms and Documents

Document Name	Status
Att 3_Published 60d FRN.pdf Supplementary Document	2008-07-01
Att 2_42 CFR Part 70.pdf Supplementary Document	2008-07-01
Att 1_Public Health Services Act.pdf Supplementary Document	2008-07-01
09-20-0171.pdf Supplementary Document	2008-06-25
09-20-0171.pdf Supplementary Document	2008-06-25
09-20-0171.pdf Supplementary Document	2008-06-25
09-20-0171.pdf Supplementary Document	2008-06-25
09-20-0171.pdf Supplementary Document	2008-06-25
09-20-0171.pdf Supplementary Document	2008-06-25
09-20-0171.pdf Supplementary Document	2008-06-25
SS_Restriction on Travel of Persons.doc Supporting Statement A	2008-07-01

IC Document Collections

IC ID	Document Title	Status
6924	Restrictions on Interstate Travel of Persons Other-WORD	Modified
185660	42 CFR 70.3 Permit Issued by State Health Authority Other-WORD	New
185659	42 CFR 70.5 Application to Move from State to State - Communicable Period (Attending Physician) Other-WORD	New
185658	42 CFR 70.5 Application to Move from State to State - Communicable Period (Traveler) Other-WORD	New
185657	42 CFR 70.4 Copy of Materials (State or Local Health Authority) Other-WORD	New
185656	42 CFR 70.4 Report by Master Vassel (Person in Charge of Conveyance) Other-WORD	New
185655	42 CFR 70.3 Copy of Materials (Applicant/Attending Physician) Other-WORD	New

ICR Details

OMB Control No: 0920-0488	ICR Reference No: 200807-0920-002
Status: Historical Active	Previous ICR Reference No: 200311-0920-001
Agency/Subagency: HHS/CDC	Agency Tracking No:
Title: Restrictions on Interstate Travel of Persons
Type of Information Collection: Reinstatement without change of a previously approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved with change	Conclusion Date: 01/08/2009
	Date Received in OIRA: 07/11/2008
Terms of Clearance: Approved for one year after which time CDC shall consult with OMB regarding the continued need for this collection of information.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	01/31/2010	36 Months From Approved
Responses	16,500	0	0
Time Burden (Hours)	3,601	0	0
Cost Burden (Dollars)	0	0	0

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Abstract: Regulations found at 42 CFR Part 70 require that a person who is in the communicable period of cholera, plague, smallpox, typhus, or yellow fever or who, having been exposed to any such disease, is in the incubation priod thereof, request a permit from the Surgeon General or his/her disignated representative to travel from one State to another, if that State has a requirement for such a permit. The regulation futher require that the master of a vessel or a person in charge of a conveyance engaged in interstate traffic, on which a suspected case of communicable disease develops shall notify the local health authority at the next port of call, station, or stop, and take such measures to prevent the spread of the disease as the local health authority directs.

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Authorizing Statute(s): US Code: 42 USC 241 Name of Law: Public Health Service Act
   US Code: 42 USC 70 Name of Law: Interstate Quarantine
  

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
	Not associated with rulemaking

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	73 FR 9340	02/20/2008
30-day Notice:	Federal Register Citation:	Citation Date:
	73 FR 36517	06/27/2008
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 7

IC Title	Form No.	Form Name
42 CFR 70.4 Report by Master Vassel (Person in Charge of Conveyance)
42 CFR 70.3 Permit Issued by State Health Authority
42 CFR 70.4 Copy of Materials (State or Local Health Authority)
42 CFR 70.5 Application to Move from State to State - Communicable Period (Attending Physician)
42 CFR 70.5 Application to Move from State to State - Communicable Period (Traveler)
Restrictions on Interstate Travel of Persons
42 CFR 70.3 Copy of Materials (Applicant/Attending Physician)

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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	16,500	0	0	16,500	0	0
Annual Time Burden (Hours)	3,601	0	0	3,601	0	0
Annual Cost Burden (Dollars)	0	0	0	0	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: No

Burden Reduction Due to:

Short Statement: This is a request for reinstatement without change of a previously approved information collection request (ICR).

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Annual Cost to Federal Government: $176,544

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? Yes

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? Uncollected

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? Uncollected

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? Uncollected

Is this ICR related to the Pandemic Response? Uncollected

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Common Form ICR:  No

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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: 07/11/2008

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