Agency Forms Undergoing Paperwork Reduction Act Review, 9475 [2016-04012]

Download as PDF Federal Register / Vol. 81, No. 37 / Thursday, February 25, 2016 / Notices Leroy A. Richardson, Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2016–04014 Filed 2–24–16; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30-Day–16–15BBT] Agency Forms Undergoing Paperwork Reduction Act Review The Centers for Disease Control and Prevention (CDC) has submitted the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995. The notice for the proposed information collection is published to obtain comments from the public and affected agencies. Written comments and suggestions from the public and affected agencies concerning the proposed collection of information are encouraged. Your comments should address any of the following: (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 or send an email to omb@cdc.gov. Written comments and/or suggestions regarding the items contained in this notice should be directed to the Attention: CDC Desk Officer, Office of Management and Budget, Washington, DC 20503 or by fax to (202) 395–5806. Written comments should be received within 30 days of this notice. Proposed Project State Unintentional Drug Overdose Reporting System (SUDORS)—New — National Center for Injury Prevention and Control (NCIPC), Centers for Disease Control and Prevention (CDC). Background and Brief Description In 2013, there were nearly 44,000 drug overdose deaths, including nearly 36,000 unintentional drug overdose deaths, in the United States. More people are now dying of drug overdose than automobile crashes in the U.S. A major driver of the problem are overdoses related to opioids, both opioid pain relievers (OPRs) and illicit forms such as heroin. In order to address this public health problem, the U.S. Department of Health and Human Services (HHS) has made addressing the opioid abuse problem a high priority. In order to support targeting of drug overdose prevention efforts, detect new trends in fatal unintentional drug 9475 overdoses, and assess the progress of HHS’s initiative to reduce opioid abuse and overdoses, the State Unintentional Drug Overdose Reporting System (SUDORS) plans to generate public health surveillance information at the national, state, and local levels that is more detailed, useful, and timely than is currently available. SUDORS will collect information that is currently not collected on death certificates such as whether the drug(s) causing the overdoses were injected or taken orally, decedent toxicology report, if available, and risk factors for fatal drug overdoses including previous drug overdoses, decedent’s mental health, and whether the decedent recently exiting a treatment program. SUDORS will leverage on the existing web-based data collection platform, the National Violent Death Reporting System (NVDRS) (OMB Control No. 0920–0607), to collect Coroner and Medical Examiner (CME) information, including toxicology, and death certificate information on unintentional fatal drug overdoses. This proposed collection will generate public health surveillance information on unintentional fatal drug overdoses. This information will help develop, inform, and assess the progress of drug overdose prevention strategies. Without this information, drug overdose efforts are often based on limited information available in the death certificate and anecdotal evidence. OMB approval is requested for three years. Participation is based on secondary data and is dependent on separate data collection efforts in each state managed by the state health departments or their bona fide agent. The estimated annual burden hours are 7,008. There are no costs to respondents. ESTIMATED ANNUALIZED BURDEN HOURS Form name Number of respondents Number of responses per respondent Average burden per response (in hours) Public Agencies .............................................. mstockstill on DSK4VPTVN1PROD with NOTICES Type of respondent Retrieving and refile records .......................... 16 876 30/60 Leroy A. Richardson, Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2016–04012 Filed 2–24–16; 8:45 am] BILLING CODE 4163–18–P VerDate Sep<11>2014 18:07 Feb 24, 2016 Jkt 238001 PO 00000 Frm 00057 Fmt 4703 Sfmt 9990 E:\FR\FM\25FEN1.SGM 25FEN1

Agencies

[Federal Register Volume 81, Number 37 (Thursday, February 25, 2016)]
[Notices]
[Page 9475]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-04012]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30-Day-16-15BBT]


Agency Forms Undergoing Paperwork Reduction Act Review

    The Centers for Disease Control and Prevention (CDC) has submitted 
the following information collection request to the Office of 
Management and Budget (OMB) for review and approval in accordance with 
the Paperwork Reduction Act of 1995. The notice for the proposed 
information collection is published to obtain comments from the public 
and affected agencies.
    Written comments and suggestions from the public and affected 
agencies concerning the proposed collection of information are 
encouraged. Your comments should address any of the following: (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 or send an email to omb@cdc.gov. Written comments and/or 
suggestions regarding the items contained in this notice should be 
directed to the Attention: CDC Desk Officer, Office of Management and 
Budget, Washington, DC 20503 or by fax to (202) 395-5806. Written 
comments should be received within 30 days of this notice.

Proposed Project

    State Unintentional Drug Overdose Reporting System (SUDORS)--New -- 
National Center for Injury Prevention and Control (NCIPC), Centers for 
Disease Control and Prevention (CDC).

Background and Brief Description

    In 2013, there were nearly 44,000 drug overdose deaths, including 
nearly 36,000 unintentional drug overdose deaths, in the United States. 
More people are now dying of drug overdose than automobile crashes in 
the U.S. A major driver of the problem are overdoses related to 
opioids, both opioid pain relievers (OPRs) and illicit forms such as 
heroin. In order to address this public health problem, the U.S. 
Department of Health and Human Services (HHS) has made addressing the 
opioid abuse problem a high priority.
    In order to support targeting of drug overdose prevention efforts, 
detect new trends in fatal unintentional drug overdoses, and assess the 
progress of HHS's initiative to reduce opioid abuse and overdoses, the 
State Unintentional Drug Overdose Reporting System (SUDORS) plans to 
generate public health surveillance information at the national, state, 
and local levels that is more detailed, useful, and timely than is 
currently available.
    SUDORS will collect information that is currently not collected on 
death certificates such as whether the drug(s) causing the overdoses 
were injected or taken orally, decedent toxicology report, if 
available, and risk factors for fatal drug overdoses including previous 
drug overdoses, decedent's mental health, and whether the decedent 
recently exiting a treatment program. SUDORS will leverage on the 
existing web-based data collection platform, the National Violent Death 
Reporting System (NVDRS) (OMB Control No. 0920-0607), to collect 
Coroner and Medical Examiner (CME) information, including toxicology, 
and death certificate information on unintentional fatal drug 
overdoses.
    This proposed collection will generate public health surveillance 
information on unintentional fatal drug overdoses. This information 
will help develop, inform, and assess the progress of drug overdose 
prevention strategies. Without this information, drug overdose efforts 
are often based on limited information available in the death 
certificate and anecdotal evidence.
    OMB approval is requested for three years. Participation is based 
on secondary data and is dependent on separate data collection efforts 
in each state managed by the state health departments or their bona 
fide agent.
    The estimated annual burden hours are 7,008. There are no costs to 
respondents.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                   Number of     Average  burden
         Type of respondent                  Form name            Number of      responses per    per  response
                                                                 respondents       respondent       (in hours)
----------------------------------------------------------------------------------------------------------------
Public Agencies.....................  Retrieving and refile                16              876            30/60
                                       records.
----------------------------------------------------------------------------------------------------------------


Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific 
Integrity, Office of the Associate Director for Science, Office of the 
Director, Centers for Disease Control and Prevention.
[FR Doc. 2016-04012 Filed 2-24-16; 8:45 am]
 BILLING CODE 4163-18-P
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