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:
0920-1335
ICR Reference No:
202310-0920-011
Status:
Active
Previous ICR Reference No:
202306-0920-002
Agency/Subagency:
HHS/CDC
Agency Tracking No:
0920-1335-24AN
Title:
[NCEZID] Phased Approach to the Resumption of Cruise Ship Passenger Operations
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:
11/01/2023
Retrieve Notice of Action (NOA)
Date Received in OIRA:
10/31/2023
Terms of Clearance:
Inventory as of this Action
Requested
Previously Approved
Expiration Date
01/31/2026
01/31/2026
01/31/2026
Responses
6,801
0
6,501
Time Burden (Hours)
2,765
0
2,715
Cost Burden (Dollars)
239,856
0
233,556
Abstract:
As part of its Phased Approach to the Resumption of Passenger Operations, CDC will collect information from cruise ships operating or intending to operate in U.S. waters. This phased approach includes increased reporting of COVID-19 and COVID-19 like illnesses as well as a number of information collections designed to ensure cruise ships can prevent, detect, and respond to outbreaks of COVID-19. This Extension of an existing Information Collection Request is submitted to allow collection to continue for an additional three years. The resumption of passenger voyages in the U.S. has facilitated the introduction and sustained transmission of COVID-19 among cruise ships, despite high vaccination rates among both crew and passengers, highlighting the continued need to temporarily extend CDC’s public health management to mitigate this risk. This Change Request is submitted to make modifications to the Cruise Ship Cumulative Acute Respiratory Illness (ARI) Reporting Form and to request a small increase in Burden Hours (51) for cruise ships to report earlier if >3% of passengers or crew are sick so that CDC can provide technical assistance in managing the outbreak, and then again at the end of the voyage to monitor progression of the outbreak.
Authorizing Statute(s):
US Code:
42 USC CFR 71
Name of Law: Foreign Quarantine
US Code:
42 USC 264
Name of Law: PHSA
US Code:
42 USC CFR 70
Name of Law: Interstate Quarantine
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:
86 FR 22964
04/30/2021
30-day Notice:
Federal Register Citation:
Citation Date:
87 FR 12706
03/07/2022
Did the Agency receive public comments on this ICR?
Yes
Number of Information Collection (IC) in this ICR:
11
IC Title
Form No.
Form Name
COVID-19 Program for Cruise Ships Notice of Participation/Nonparticipation
0920-1335
Attachment E_Notice of Participation-Nonparticipation
Cruise Ship Brand/Operator - Agreement with Health Care Organization with signoff from Local Health Authorities
0920-1335
Attachment N_Agreement with Health Care Organization
Cruise Ship Brand/Operator - Agreement with Housing Facility with signoff from Local Health Authorities
0920-1335
Attachment O_Agreement with Housing Facility
Cruise Ship Holding Company - COVID-19 Response Plan
Cruise Ship Operator - Agreement with Port of Entry with signoff from Local Health Authority
0920-1335
Attachment M_Agreement with Port of Entry
Cruise Ship Operator - Remote and In-person Inspections
Cruise Ship Physician - COVID-19 Case Investigation Worksheet (if necessary)
0920-1335, 0920-1335
COVID-19 Case Investigation worksheet
,
Attachment K_Cruise COVID19 Case Investigation Worksheet
Cruise Ship Physician - COVID-19 Contact Investigation Worksheet (if necessary)
0920-1335
Attachment L_Cruise COVID19 Contact Investigation Worksheet
Cruise Ship Physician - Cruise Ship Cumulative Acute Respiratory Illness (ARI) Reporting Form (submitted once per voyage, within 24 hours before arrival in U.S.)
None, 0920-1335
Cruise Ship Cumulative Acute Respiratory Illness (ARI) Reporting Form
,
Cruise Ship Cumulative Acute Respiratory Illness (ARI) Reporting Form (submitted once per voyage, within 24 hours before arrival in U.S.)
Cruise Ship Physician - Cruise Ship Cumulative Acute Respiratory Illness (submitted sooner than 24 hours before arrival in U.S because 3% or more of the voyage's passengers or crew have ARI)
0920-1335
Cruise Ship Physician - Cruise Ship Cumulative Acute Respiratory Illness (submitted sooner than 24 hours before arrival in U.S because 3% or more of the voyage’s passengers or crew have ARI)
Cruise Ship Vaccination Status Classification
0920-1335
Attachment F_Cruise Ship Vaccination Status Classification
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
6,801
6,501
0
300
0
0
Annual Time Burden (Hours)
2,765
2,715
0
50
0
0
Annual Cost Burden (Dollars)
239,856
233,556
0
6,300
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:
Change Request for 0920-1335 submitted to modify Cruise Ship Cumulative Acute Respiratory Illness (ARI) Reporting Form and to request a small increase in Burden Hours (51) due to cruise ship reporting requirements.
Annual Cost to Federal Government:
$1,477,542
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?
Yes
Agency Contact:
Jeffrey Zirger 404 639-7118 wtj5@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:
10/31/2023
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