Proposed Data Collection Submitted for Public Comment and Recommendations, 20476-20477 [2024-06094]

Download as PDF 20476 Federal Register / Vol. 89, No. 57 / Friday, March 22, 2024 / Notices and Prevention, 4770 Buford Highway, Mailstop S106–3, Atlanta, Georgia 30341–3717. Telephone: (404) 639– 4601; email: NBrown3@cdc.gov. SUPPLEMENTARY INFORMATION: Notice is hereby given of a change in the meeting of the Disease, Disability, and Injury Prevention and Control Special Emphasis Panel (SEP)—SIP24–009, Arthritis Management and Wellbeing Network (AMWN); May 15, 2024, 10 a.m.–6 p.m., EDT, teleconference/web conference, in the original Federal Register notice. The meeting notice was published in the Federal Register on February 13, 2024, 89 FR 10080. This meeting notice is being corrected to change the Notice of Funding Opportunity (NOFO) title and should read as follows: Name of Committee: Disease, Disability, and Injury Prevention and Control Special Emphasis Panel (SEP)— SIP24–009, Arthritis Management and Wellbeing Research Network (AMWRN). The meeting is closed to the public. The Director, Office of Strategic Business Initiatives, Office of the Chief Operating Officer, Centers for Disease Control and Prevention, has been delegated the authority to sign Federal Register notices pertaining to announcements of meetings and other committee management activities, for both the Centers for Disease Control and Prevention and the Agency for Toxic Substances and Disease Registry. Kalwant Smagh, Director, Office of Strategic Business Initiatives, Office of the Chief Operating Officer, Centers for Disease Control and Prevention. [FR Doc. 2024–06058 Filed 3–21–24; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day–24–24DU; Docket No. CDC–2024– 0021] Proposed Data Collection Submitted for Public Comment and Recommendations Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). ACTION: Notice with comment period. ddrumheller on DSK120RN23PROD with NOTICES1 AGENCY: The Centers for Disease Control and Prevention (CDC), as part of its continuing effort to reduce public burden and maximize the utility of government information, invites the general public and other federal SUMMARY: VerDate Sep<11>2014 19:15 Mar 21, 2024 Jkt 262001 agencies the opportunity to comment on a proposed information collection, as required by the Paperwork Reduction Act of 1995. This notice invites comment on a proposed information collection project titled Generic Clearance for the Collection of Minimal Data Necessary for Case Data During an Emergency Response. This information collection will allow CDC to collect the minimum data necessary for confirmed, probable, and suspected cases of any disease or condition that is the subject of an emergency response. DATES: CDC must receive written comments on or before May 21, 2024. ADDRESSES: You may submit comments, identified by Docket No. CDC–2024– 0021 by either of the following methods: • Federal eRulemaking Portal: www.regulations.gov. Follow the instructions for submitting comments. • Mail: Jeffrey M. Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS H21–8, Atlanta, Georgia 30329. Instructions: All submissions received must include the agency name and Docket Number. CDC will post, without change, all relevant comments to www.regulations.gov. Please note: Submit all comments through the Federal eRulemaking portal (www.regulations.gov) or by U.S. mail to the address listed above. FOR FURTHER INFORMATION CONTACT: To request more information on the proposed project or to obtain a copy of the information collection plan and instruments, contact Jeffrey M. Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS H21–8, Atlanta, Georgia 30329; Telephone: 404–639–7570; Email: omb@ cdc.gov. SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501–3520), federal agencies must obtain approval from the Office of Management and Budget (OMB) for each collection of information they conduct or sponsor. In addition, the PRA also requires federal agencies to provide a 60-day notice in the Federal Register concerning each proposed collection of information, including each new proposed collection, each proposed extension of existing collection of information, and each reinstatement of previously approved information collection before submitting the collection to the OMB for approval. To comply with this requirement, we are publishing this notice of a proposed data collection as described below. PO 00000 Frm 00054 Fmt 4703 Sfmt 4703 The OMB is particularly interested in comments that will help: 1. Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; 2. Evaluate the accuracy of the agency’s estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; 3. Enhance the quality, utility, and clarity of the information to be collected; 4. 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 submissions of responses; and 5. Assess information collection costs. Proposed Project Generic Clearance for the Collection of Minimal Data Necessary for Case Data During an Emergency Response—New— Office of Public Health Data, Surveillance, and Technology (OPHDST), Centers for Disease Control and Prevention (CDC). Background and Brief Description During a public health emergency response, state, tribal, local, and territorial (STLT) health departments and CDC need to exchange data on confirmed, probable, and suspected cases rapidly. Timely notifications of cases from STLT to CDC are critical to provide situational awareness at the federal level to support decision making, particularly for public health threats that escalate quickly and cross jurisdictions. To this end, collecting the minimum data necessary will provide standardization and consistency among technical approaches and Agency-wide processes. The harmonization across CDC programs and STLTs will reduce the burden on STLTs and healthcare providers from ad hoc requests for case data from CDC programs. Section 319D of the Public Health Service Act (as amended Through Pub. L. 118–35, enacted January 19, 2024) states that CDC shall define the minimum data necessary as the Agency collaborates with STLTs and other partners to improve the appropriate near real-time electronic transmission of interoperable public health data for situational awareness and response to public health emergencies. In addition, the CDC Advisory Committee to the E:\FR\FM\22MRN1.SGM 22MRN1 20477 Federal Register / Vol. 89, No. 57 / Friday, March 22, 2024 / Notices Director (ACD) recommends that CDC should establish the minimum data necessary for core data sources including case data to be transmitted to CDC from STLTs. CDC requests a three-year approval for a New Generic Information Collection Request (ICR), for the Collection of Minimal Data Necessary for Case Data During an Emergency Response. This new ICR includes a request for approval for CDC to collect the minimum data necessary for confirmed, probable, and suspected cases of any disease or condition that is the subject of an emergency response. Data may be sent to CDC by STLT health departments travel histories and other information to describe and manage outbreaks and conduct public health follow-up to minimize the spread of disease. The burden estimates include the time that states, territories, freely associated states, and cities will incur to submit confirmed, probable, and suspected case data for diseases or conditions that are the subject of an emergency response. The estimated annual burden for the 60 respondents is 10,951 hours. There is no cost to respondents other than their time to participate. through the National Notifiable Diseases Surveillance System (NNDSS), Data Collation and Integration for Public Health Event Response (DCIPHER), or other automated or non-automated mechanisms including but not limited to fax, email, secure file upload, and data entry to a secure website. Data will be used for ongoing situational awareness and to monitor the occurrence and spread of the disease or condition. Other uses may include identifying populations or geographic areas at high risk; planning prevention and control programs and policies; and allocating resources appropriately. The data may also be used by CDC to obtain ESTIMATED ANNUALIZED BURDEN HOURS Type of respondent States ................................................ Territories .......................................... Freely Associated States .................. Cities ................................................. Total ........................................... Submission Submission Submission Submission 50 5 3 2 365 365 365 365 30/60 30/60 30/60 30/60 9,125 913 548 365 ........................................................... ........................ ........................ ........................ 10,951 [FR Doc. 2024–06094 Filed 3–21–24; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day–24–23HM] ddrumheller on DSK120RN23PROD with NOTICES1 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 ‘‘Assessing Fatigue and Fatigue Management in U.S. Onshore Oil and Gas Extraction’’ 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 August 21, 2023 to obtain comments from the public and affected agencies. CDC did not receive comments related to the previous notice. This notice serves to allow an additional 30 VerDate Sep<11>2014 19:15 Mar 21, 2024 Jkt 262001 case case case case data data data data Total burden (in hours) .................. .................. .................. .................. Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Public Health Ethics and Regulations, Office of Science, Centers for Disease Control and Prevention. of of of of Average burden per response (in hours) Number of responses per respondent Number of respondents Form name 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 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 PO 00000 Frm 00055 Fmt 4703 Sfmt 4703 proposed information collection should be sent within 30 days of publication of this notice to www.reginfo.gov/public/ do/PRAMain. 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 Assessing Fatigue and Fatigue Management in U.S. Onshore Oil and Gas Extraction—New—National Institute for Occupational Safety and Health (NIOSH), Centers for Disease Control and Prevention (CDC). Background and Brief Description Oil and gas extraction (OGE) workers play an important role in supporting the United States economy and help fulfill the energy needs of Americans and American businesses. OGE workers have significant risks for a variety of exposures at oil and gas well sites. There has been no significant fatigue research in the United States onshore upstream OGE sector. This proposed project will characterize relationships E:\FR\FM\22MRN1.SGM 22MRN1

Agencies

[Federal Register Volume 89, Number 57 (Friday, March 22, 2024)]
[Notices]
[Pages 20476-20477]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-06094]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[60Day-24-24DU; Docket No. CDC-2024-0021]


Proposed Data Collection Submitted for Public Comment and 
Recommendations

AGENCY: Centers for Disease Control and Prevention (CDC), Department of 
Health and Human Services (HHS).

ACTION: Notice with comment period.

-----------------------------------------------------------------------

SUMMARY: The Centers for Disease Control and Prevention (CDC), as part 
of its continuing effort to reduce public burden and maximize the 
utility of government information, invites the general public and other 
federal agencies the opportunity to comment on a proposed information 
collection, as required by the Paperwork Reduction Act of 1995. This 
notice invites comment on a proposed information collection project 
titled Generic Clearance for the Collection of Minimal Data Necessary 
for Case Data During an Emergency Response. This information collection 
will allow CDC to collect the minimum data necessary for confirmed, 
probable, and suspected cases of any disease or condition that is the 
subject of an emergency response.

DATES: CDC must receive written comments on or before May 21, 2024.

ADDRESSES: You may submit comments, identified by Docket No. CDC-2024-
0021 by either of the following methods:
     Federal eRulemaking Portal: www.regulations.gov. Follow 
the instructions for submitting comments.
     Mail: Jeffrey M. Zirger, Information Collection Review 
Office, Centers for Disease Control and Prevention, 1600 Clifton Road 
NE, MS H21-8, Atlanta, Georgia 30329.
    Instructions: All submissions received must include the agency name 
and Docket Number. CDC will post, without change, all relevant comments 
to www.regulations.gov.
    Please note: Submit all comments through the Federal eRulemaking 
portal (www.regulations.gov) or by U.S. mail to the address listed 
above.

FOR FURTHER INFORMATION CONTACT: To request more information on the 
proposed project or to obtain a copy of the information collection plan 
and instruments, contact Jeffrey M. Zirger, Information Collection 
Review Office, Centers for Disease Control and Prevention, 1600 Clifton 
Road NE, MS H21-8, Atlanta, Georgia 30329; Telephone: 404-639-7570; 
Email: [email protected].

SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995 
(PRA) (44 U.S.C. 3501-3520), federal agencies must obtain approval from 
the Office of Management and Budget (OMB) for each collection of 
information they conduct or sponsor. In addition, the PRA also requires 
federal agencies to provide a 60-day notice in the Federal Register 
concerning each proposed collection of information, including each new 
proposed collection, each proposed extension of existing collection of 
information, and each reinstatement of previously approved information 
collection before submitting the collection to the OMB for approval. To 
comply with this requirement, we are publishing this notice of a 
proposed data collection as described below.
    The OMB is particularly interested in comments that will help:
    1. Evaluate whether the proposed collection of information is 
necessary for the proper performance of the functions of the agency, 
including whether the information will have practical utility;
    2. Evaluate the accuracy of the agency's estimate of the burden of 
the proposed collection of information, including the validity of the 
methodology and assumptions used;
    3. Enhance the quality, utility, and clarity of the information to 
be collected;
    4. 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 
submissions of responses; and
    5. Assess information collection costs.

Proposed Project

    Generic Clearance for the Collection of Minimal Data Necessary for 
Case Data During an Emergency Response--New--Office of Public Health 
Data, Surveillance, and Technology (OPHDST), Centers for Disease 
Control and Prevention (CDC).

Background and Brief Description

    During a public health emergency response, state, tribal, local, 
and territorial (STLT) health departments and CDC need to exchange data 
on confirmed, probable, and suspected cases rapidly. Timely 
notifications of cases from STLT to CDC are critical to provide 
situational awareness at the federal level to support decision making, 
particularly for public health threats that escalate quickly and cross 
jurisdictions. To this end, collecting the minimum data necessary will 
provide standardization and consistency among technical approaches and 
Agency-wide processes. The harmonization across CDC programs and STLTs 
will reduce the burden on STLTs and healthcare providers from ad hoc 
requests for case data from CDC programs.
    Section 319D of the Public Health Service Act (as amended Through 
Pub. L. 118-35, enacted January 19, 2024) states that CDC shall define 
the minimum data necessary as the Agency collaborates with STLTs and 
other partners to improve the appropriate near real-time electronic 
transmission of interoperable public health data for situational 
awareness and response to public health emergencies. In addition, the 
CDC Advisory Committee to the

[[Page 20477]]

Director (ACD) recommends that CDC should establish the minimum data 
necessary for core data sources including case data to be transmitted 
to CDC from STLTs.
    CDC requests a three-year approval for a New Generic Information 
Collection Request (ICR), for the Collection of Minimal Data Necessary 
for Case Data During an Emergency Response. This new ICR includes a 
request for approval for CDC to collect the minimum data necessary for 
confirmed, probable, and suspected cases of any disease or condition 
that is the subject of an emergency response. Data may be sent to CDC 
by STLT health departments through the National Notifiable Diseases 
Surveillance System (NNDSS), Data Collation and Integration for Public 
Health Event Response (DCIPHER), or other automated or non-automated 
mechanisms including but not limited to fax, email, secure file upload, 
and data entry to a secure website.
    Data will be used for ongoing situational awareness and to monitor 
the occurrence and spread of the disease or condition. Other uses may 
include identifying populations or geographic areas at high risk; 
planning prevention and control programs and policies; and allocating 
resources appropriately. The data may also be used by CDC to obtain 
travel histories and other information to describe and manage outbreaks 
and conduct public health follow-up to minimize the spread of disease.
    The burden estimates include the time that states, territories, 
freely associated states, and cities will incur to submit confirmed, 
probable, and suspected case data for diseases or conditions that are 
the subject of an emergency response. The estimated annual burden for 
the 60 respondents is 10,951 hours. There is no cost to respondents 
other than their time to participate.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                     Number of    Average burden
      Type of respondent            Form name        Number of     responses per   per response    Total burden
                                                    respondents     respondent      (in hours)      (in hours)
----------------------------------------------------------------------------------------------------------------
States........................  Submission of                 50             365           30/60           9,125
                                 case data.
Territories...................  Submission of                  5             365           30/60             913
                                 case data.
Freely Associated States......  Submission of                  3             365           30/60             548
                                 case data.
Cities........................  Submission of                  2             365           30/60             365
                                 case data.
                                                 ---------------------------------------------------------------
    Total.....................  ................  ..............  ..............  ..............          10,951
----------------------------------------------------------------------------------------------------------------


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. 2024-06094 Filed 3-21-24; 8:45 am]
BILLING CODE 4163-18-P


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