Proposed Data Collection Submitted for Public Comment and Recommendations, 24004-24005 [2024-07287]

Download as PDF 24004 Federal Register / Vol. 89, No. 67 / Friday, April 5, 2024 / Notices of Multiple Forms of Violence.’’ Agenda items are subject to change as priorities dictate. 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. Please note: Submit all comments through the Federal eRulemaking portal (www.regulations.gov) or by U.S. mail to the address listed above. [FR Doc. 2024–07300 Filed 4–4–24; 8:45 am] BILLING CODE 4163–18–P FOR FURTHER INFORMATION CONTACT: DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day–24–24EE; Docket No. CDC–2024– 0023] 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. 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 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 DFWED National Hypothesis Generation and Investigation Module. The proposed data collection will define a core set of standardized data elements and forms used for outbreak investigations and surveillance activities for a variety of enteric illnesses. khammond on DSKJM1Z7X2PROD with NOTICES SUMMARY: VerDate Sep<11>2014 16:44 Apr 04, 2024 Jkt 262001 CDC must receive written comments on or before June 4, 2024. ADDRESSES: You may submit comments, identified by Docket No. CDC–2024– 0023 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. DATES: 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. 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 PO 00000 Frm 00044 Fmt 4703 Sfmt 4703 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 DFWED National Hypothesis Generation and Investigation Module— New—National Center for Emerging and Zoonotic Infectious Diseases (NCEZID), Centers for Disease Control and Prevention (CDC). Background and Brief Description The Division of Foodborne, Waterborne, and Environmental Diseases (DFWED) at the Centers for Disease Control and Prevention (CDC) aims to protect public health through the prevention and control of disease, disability, and death caused by foodborne, enteric, waterborne, and environmentally transmitted infections. To overcome challenges presented by the changing landscape of enteric diseases, the need for comprehensive hypothesis generating questionnaires focused on a range of settings, activities, and potential modes of transmission are essential to guide prevention and control activities. The submitted forms standardize hypothesis generating instruments used during enteric disease outbreak investigations and surveillance. This includes foodborne, waterborne, and zoonotic disease surveillance and outbreak investigations. In addition, enhanced surveillance for antibiotic resistant isolates is also included in this package. CDC requests OMB approval for an estimated 5,852 annual burden hours. There is no cost to respondents other than their time to participate. E:\FR\FM\05APN1.SGM 05APN1 24005 Federal Register / Vol. 89, No. 67 / Friday, April 5, 2024 / Notices ESTIMATED ANNUALIZED BURDEN HOURS Form name Cluster and outbreak case patients .............. National Hypothesis Generating Questionnaire. Foodborne Focus Questionnaire. Animal Contact Focus Questionnaire. Shigella Hypothesis Generating Questionnaire. NARMS SIRI Questionnaire Module 1. Cluster and outbreak case patients .............. Cluster and outbreak case patients .............. Shigellosis case patients .............................. Nontyphoidal Salmonella, STEC, Vibrio, or Campylobacter case patients whose bacterial isolates have concerning antimicrobial resistance. Nontyphoidal Salmonella (except Newport strain), STEC, or Vibrio case patients whose bacterial isolates have concerning antimicrobial resistance. Multidrug-resistant Salmonella Newport case patients. Campylobacter case patients whose bacterial isolates have concerning antimicrobial resistance. Salmonella Typhi or Paratyphi case patients whose bacterial isolates have concerning antimicrobial resistance. Total ....................................................... 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. 2024–07287 Filed 4–4–24; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES [60Day–24–0556; Docket No. CDC–2024– 0025] 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. 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 agencies the opportunity to comment on a continuing information collection, as required by the Paperwork Reduction Act of 1995. This notice invites comment on a proposed information SUMMARY: VerDate Sep<11>2014 16:44 Apr 04, 2024 Jkt 262001 Number of responses per respondent Average burden per response (in hours) Total burden hours 4,000 1 45/60 3,000 4,000 1 20/60 1,333 450 1 30 min 225 1500 1 45/60 1,125 305 1 15/60 77 NARMS SIRI Questionnaire Module 2. 130 1 10/60 22 NARMS SIRI Questionnaire Module 3. NARMS SIRI Questionnaire Module 4. 125 1 15/60 32 50 1 25/60 21 NARMS SIRI Questionnaire Module 5. 50 1 20/60 17 ........................ ........................ ........................ 5,852 ............................................... collection project titled Assisted Reproductive Technology (ART) Program Reporting System. This study is designed to collect information on ART cycles to publish information on pregnancy success rates as required under Section 2(a) of the Federal Clinic Success Rate and Certification Act (FCSRCA). CDC must receive written comments on or before June 4, 2024. ADDRESSES: You may submit comments, identified by Docket No. CDC–2024– 0025 by either of the following methods: b Federal eRulemaking Portal: www.regulations.gov. Follow the instructions for submitting comments. b 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. DATES: Centers for Disease Control and Prevention khammond on DSKJM1Z7X2PROD with NOTICES Number of respondents Type of respondents Please note: Submit all comments through the Federal eRulemaking portal (www.regulations.gov) or by U.S. mail to the address listed above. To request more information on the proposed project or to obtain a copy of the information collection plan and FOR FURTHER INFORMATION CONTACT: PO 00000 Frm 00045 Fmt 4703 Sfmt 4703 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: 404–639–7118; Email: omb@ cdc.gov. 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; SUPPLEMENTARY INFORMATION: E:\FR\FM\05APN1.SGM 05APN1

Agencies

[Federal Register Volume 89, Number 67 (Friday, April 5, 2024)]
[Notices]
[Pages 24004-24005]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-07287]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[60Day-24-24EE; Docket No. CDC-2024-0023]


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 DFWED National Hypothesis Generation and Investigation Module. 
The proposed data collection will define a core set of standardized 
data elements and forms used for outbreak investigations and 
surveillance activities for a variety of enteric illnesses.

DATES: CDC must receive written comments on or before June 4, 2024.

ADDRESSES: You may submit comments, identified by Docket No. CDC-2024-
0023 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

    DFWED National Hypothesis Generation and Investigation Module--
New--National Center for Emerging and Zoonotic Infectious Diseases 
(NCEZID), Centers for Disease Control and Prevention (CDC).

Background and Brief Description

    The Division of Foodborne, Waterborne, and Environmental Diseases 
(DFWED) at the Centers for Disease Control and Prevention (CDC) aims to 
protect public health through the prevention and control of disease, 
disability, and death caused by foodborne, enteric, waterborne, and 
environmentally transmitted infections. To overcome challenges 
presented by the changing landscape of enteric diseases, the need for 
comprehensive hypothesis generating questionnaires focused on a range 
of settings, activities, and potential modes of transmission are 
essential to guide prevention and control activities. The submitted 
forms standardize hypothesis generating instruments used during enteric 
disease outbreak investigations and surveillance. This includes 
foodborne, waterborne, and zoonotic disease surveillance and outbreak 
investigations. In addition, enhanced surveillance for antibiotic 
resistant isolates is also included in this package.
    CDC requests OMB approval for an estimated 5,852 annual burden 
hours. There is no cost to respondents other than their time to 
participate.

[[Page 24005]]



                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                     Number of    Average burden
      Type of respondents           Form name        Number of     responses per   per response    Total burden
                                                    respondents     respondent      (in hours)         hours
----------------------------------------------------------------------------------------------------------------
Cluster and outbreak case       National                   4,000               1           45/60           3,000
 patients.                       Hypothesis
                                 Generating
                                 Questionnaire.
Cluster and outbreak case       Foodborne Focus            4,000               1           20/60           1,333
 patients.                       Questionnaire.
Cluster and outbreak case       Animal Contact               450               1          30 min             225
 patients.                       Focus
                                 Questionnaire.
Shigellosis case patients.....  Shigella                    1500               1           45/60           1,125
                                 Hypothesis
                                 Generating
                                 Questionnaire.
Nontyphoidal Salmonella, STEC,  NARMS SIRI                   305               1           15/60              77
 Vibrio, or Campylobacter case   Questionnaire
 patients whose bacterial        Module 1.
 isolates have concerning
 antimicrobial resistance.
Nontyphoidal Salmonella         NARMS SIRI                   130               1           10/60              22
 (except Newport strain),        Questionnaire
 STEC, or Vibrio case patients   Module 2.
 whose bacterial isolates have
 concerning antimicrobial
 resistance.
Multidrug-resistant Salmonella  NARMS SIRI                   125               1           15/60              32
 Newport case patients.          Questionnaire
                                 Module 3.
Campylobacter case patients     NARMS SIRI                    50               1           25/60              21
 whose bacterial isolates have   Questionnaire
 concerning antimicrobial        Module 4.
 resistance.
Salmonella Typhi or Paratyphi   NARMS SIRI                    50               1           20/60              17
 case patients whose bacterial   Questionnaire
 isolates have concerning        Module 5.
 antimicrobial resistance.
                                                 ---------------------------------------------------------------
    Total.....................  ................  ..............  ..............  ..............           5,852
----------------------------------------------------------------------------------------------------------------


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. 2024-07287 Filed 4-4-24; 8:45 am]
BILLING CODE 4163-18-P


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