View Information Collection Request (ICR) Package
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View ICR - Agency Submission
COMMENT
Time Remaining
Days
HR
Min
Sec
OMB Control No:
0920-1335
ICR Reference No:
202603-0920-015
Status:
Received in OIRA
Previous ICR Reference No:
202310-0920-011
Agency/Subagency:
HHS/CDC
Agency Tracking No:
0920-26-0163
Title:
[NCEZID] Maritime-related Public Health Activities
Type of Information Collection:
Reinstatement with change of a previously approved collection
Common Form ICR:
No
Type of Review Request:
Regular
Date Submitted to OIRA:
04/14/2026
Requested
Previously Approved
Expiration Date
36 Months From Approved
Responses
4,991
0
Time Burden (Hours)
836
0
Cost Burden (Dollars)
0
0
Abstract:
The purpose of this activity is to collect data related to maritime travelers involved with exposure or contraction of disease when traveling. Respondents include operators of all commercial passenger-carrying vessels, cargo ships, international ferries, fishing boats, and research vessels that seek to operate in international waterways and subject to the jurisdiction of the United States. Some data are required such as reports of ill persons (defined in 42 CFR Part 71.1) and deaths (42 CFR Part 71.21, 70.4, and 70.35). Other information collections help CDC understand risk and facilitate assistance to ships. This is a Reinstatement with Change that includes removal and addition of instruments and a burden decrease.
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:
91 FR 1794
01/15/2026
30-day Notice:
Federal Register Citation:
Citation Date:
91 FR 19137
04/14/2026
Did the Agency receive public comments on this ICR?
Yes
Number of Information Collection (IC) in this ICR:
9
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 Cumulative Acute Respiratory Illness (ARI) Reporting Form (submitted once per voyage, within 24 hours before arrival in U.S.)
n/a
Cruise Ship Cumulative Acute Respiratory Illness (ARI) Reporting Form
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)
n/a
Cruise Ship Cumulative Acute Respiratory Illness (ARI) Reporting Form
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 Vaccination Status Classification
0920-1335
Attachment F_Cruise Ship Vaccination Status Classification
General Maritime Contact Investigation Outcome Reporting Form
n/a
General Maritime Contact Investigation Outcome Reporting Worksheet
Maritime Conveyance Illness or Death Investigation Form [Section 5]
n/a
Maritime Conveyance Illness or Death Investigation Form
Maritime Conveyance Illness or Death Investigation Form [Sections 1-4]
n/a
Maritime Conveyance Illness or Death Investigation Form
Report of Death Illness During Stay in Port (Verbal-No Form)
Report of Death Illness from Ship (Verbal-No Form)
TB Maritime Contact Investigation Worksheet
n/a
TB Maritime Investigation Worksheet
Varicella Outbreak Enhanced Data Collection Form - Maritime
n/a
Varicella Outbreak Reporting Form
ICR Summary of Burden
Total Request
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
4,991
0
0
4,490
0
501
Annual Time Burden (Hours)
836
0
0
-879
0
1,715
Annual Cost Burden (Dollars)
0
0
0
-107,556
0
107,556
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:
Yes
Burden Reduction Due to:
Changing Forms
Short Statement:
The reduction in burden is due to addition/removal of instruments and adjustment to respondent numbers.
Annual Cost to Federal Government:
$211,616
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.
Yes
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:
Kevin Joyce 404 639-1944 kdj7@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:
04/14/2026
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