Notice2026-00999

Agency Forms Undergoing Paperwork Reduction Act Review

Primary source

Metadata and text below are from the Federal Register, a public-domain U.S. government work. Always verify the official published version before relying on it for any legal matter.

Published
January 20, 2026

Issuing agencies

Health and Human Services DepartmentCenters for Disease Control and Prevention

Full Text

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<title>Federal Register, Volume 91 Issue 12 (Tuesday, January 20, 2026)</title>
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[Federal Register Volume 91, Number 12 (Tuesday, January 20, 2026)]
[Notices]
[Pages 2358-2359]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2026-00999]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30Day-26-0009]


Agency Forms Undergoing Paperwork Reduction Act Review

    In accordance with the Paperwork Reduction Act of 1995, the Centers 
for Disease Control and Prevention (CDC) has submitted the information 
collection request titled ``National Disease Surveillance Program--I. 
Case Reports'' to the Office of Management and Budget (OMB) for review 
and approval. CDC previously published a ``Proposed Data Collection 
Submitted for Public Comment and Recommendations'' notice on July 28, 
2025, to obtain comments from the public and affected agencies. CDC 
received three comments related to the previous notice. This notice 
serves to allow an additional 30 days for public and affected agency 
comments.
    CDC will accept all comments for this proposed information 
collection project. The Office of Management and Budget is particularly 
interested in comments that:
    (a) Evaluate whether the proposed collection of information is 
necessary for the proper performance of the

[[Page 2359]]

functions of the agency, including whether the information will have 
practical utility;
    (b) Evaluate the accuracy of the agencies estimate of the burden of 
the proposed collection of information, including the validity of the 
methodology and assumptions used;
    (c) Enhance the quality, utility, and clarity of the information to 
be collected;
    (d) Minimize the burden of the collection of information on those 
who are to respond, including, through the use of appropriate 
automated, electronic, mechanical, or other technological collection 
techniques or other forms of information technology, e.g., permitting 
electronic submission of responses; and
    (e) Assess information collection costs.
    To request additional information on the proposed project or to 
obtain a copy of the information collection plan and instruments, call 
(404) 639-7570. Comments and recommendations for the proposed 
information collection should be sent within 30 days of publication of 
this notice to <a href="http://www.reginfo.gov/public/do/PRAMain">www.reginfo.gov/public/do/PRAMain</a> Find this particular 
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function. Direct 
written comments and/or suggestions regarding the items contained in 
this notice to the Attention: CDC Desk Officer, Office of Management 
and Budget, 725 17th Street NW, Washington, DC 20503 or by fax to (202) 
395-5806. Provide written comments within 30 days of notice 
publication.

Proposed Project

    National Disease Surveillance Program--I. Case Reports (OMB Control 
No. 0920-0009, Exp. 1/31/2026)--Revision--National Center for Emerging 
and Zoonotic Infectious Diseases (NCEZID), Centers for Disease Control 
and Prevention (CDC).

Background and Brief Description

    Surveillance of the incidence and distribution of disease has been 
an important function of the US Public Health Service (PHS) since the 
1878 Act of Congress authorized the PHS to collect morbidity reports. 
After the Malaria Control in War Areas Program had fulfilled its 
original 1942 objective of reducing malaria transmission, its basic 
tenets were carried forward and broadened by the formation of the 
Communicable Disease Center (CDC) in 1946. CDC was conceived of as a 
well-equipped, broadly staffed agency used to translate facts about 
analysis of morbidity and mortality statistics on communicable diseases 
and through field investigations.
    It was soon recognized that control measures (such as the DDT 
spraying for malaria) did not alleviate the threat of disease 
reintroduction. In 1950, the Malaria Surveillance Program began and in 
1952, the National Surveillance Program started. Both programs were 
based on the premise that diseases cannot be diagnosed, prevented, or 
controlled until existing knowledge is expanded and new ideas developed 
and implemented. The original scope of the National Surveillance 
Program included the study of malaria, murine typhus, smallpox, 
psittacosis, diphtheria, leprosy, and sylvatic plague. Over the years, 
the mandate of CDC has broadened in preventive health activities and 
the surveillance systems maintained have expanded. This program is 
authorized under the Public Health Service Act, Section 301 and 306 (42 
U.S.C. 241 and 242K).
    This data collection covers surveillance activities for four, rare 
diseases: (1) Creutzfeldt-Jakob Disease (CJD); (2) Reye Syndrome; (3) 
Kawasaki syndrome; and (4) Acute Flaccid Myelitis. Data will be used 
for planning and evaluating effective programs for prevention and 
control of these infectious diseases. Disease incidence is needed to 
study present and emerging disease problems and the surveillance data 
serves as statistical material for those engaged in research or medical 
practice, aid to health education officials and students, and data for 
manufacturers of pharmaceutical products. Annual surveillance data are 
published in the MMWR Surveillance Summary. Case data will be 
transmitted to CDC electronically or hard copy from State and Local 
Health Departments.
    This Revision is submitted to renew the data collection package for 
an additional three years and to update the Acute Flaccid Myelitis 
format for collecting race and ethnicity. CDC requests OMB approval for 
an estimated 98 annual burden hours. There is no cost to respondents 
other than their time to participate.

                                        Estimated Annualized Burden Hours
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                                                                                     Number of    Average burden
          Type of respondents                   Form name            Number of     responses per   per response
                                                                    respondents     respondent      (in hours)
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Epidemiologist........................  Creutzfeldt-Jakob                     10               2           20/60
                                         Disease (CJD).
                                        Reye Syndrome...........               1               1           20/60
                                        Kawasaki syndrome.......              20               2           15/60
                                        Acute Flaccid Myelitis..              60               2           30/60
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Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Public Health 
Ethics and Regulations, Office of Science, Centers for Disease Control 
and Prevention.
[FR Doc. 2026-00999 Filed 1-16-26; 8:45 am]
BILLING CODE 4163-18-P


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Indexed from Federal Register on January 20, 2026.

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