Agency Information Collection Request. 60-Day Public Comment Request

<NOTICE> DEPARTMENT OF HEALTH AND HUMAN SERVICES <DEPDOC>[Document Identifier: OS-0990-new]</DEPDOC> <SUBJECT>Agency Information Collection Request. 60-Day Public Comment Request</SUBJECT> <HD SOURCE="HED">AGENCY:</HD> Office of the Secretary, HHS. <HD SOURCE="HED">ACTION:</HD> Notice. <SUM> <HD SOURCE="HED">SUMMARY:</HD> In compliance with the requirement of the Paperwork Reduction Act of 1995, the Office of the Secretary (OS), Department of Health and Human Services, is publishing the following summary of a proposed collection for public comment. </SUM> <DATES> <HD SOURCE="HED">DATES:</HD> Comments on the ICR must be received on or before April 9, 2024. </DATES> <HD SOURCE="HED">ADDRESSES:</HD> Submit your comments to <E T="03">Sherrette.Funn@hhs.gov</E> or by calling (202) 264-0041 and <E T="03">PRA@HHS.GOV</E> . <FURINF> <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD> When submitting comments or requesting information, please include the document identifier 0990-New-60D and project title for reference, to Sherrette A. Funn, email: <E T="03">Sherrette.Funn@hhs.gov, PRA@HHS.GOV</E> or call (202) 264-0041 the Reports Clearance Officer. </FURINF> <SUPLINF> <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD> Interested persons are invited to send comments regarding this burden estimate or any other aspect of this collection of information, including any of the following subjects: (1) The necessity and utility of the proposed information collection for the proper performance of the agency's functions; (2) the accuracy of the estimated burden; (3) ways to enhance the quality, utility, and clarity of the information to be collected; and (4) the use of automated collection techniques or other forms of information technology to minimize the information collection burden. <E T="03">Title of the Collection:</E> Research Misconduct and Noncompliance in Clinical Trials and Translational Research. <E T="03">Type of Collection:</E> New. <E T="03">OMB No.:</E> 0990-XXXX. <E T="03">Abstract:</E> The Department of Health and Human Services (HHS) Office of Research Integrity (ORI) has partnered with the Office for Human Research Protections (OHRP) to launch this data collection effort to better understand how to serve those who might benefit from additional education and resources to improve research integrity. ORI and OHRP have found that researchers, Institutional Review Board (IRB) Chairs, Research Integrity Officers (RIOs), Human Protections and Compliance Officers, and Human Protections Administrators, who oversee the conduct of research involving human research subjects, may struggle with identifying reportable noncompliance or unanticipated problems, protocol violations, protocol deficiencies, and falsifications and fabrications of data and methods in that research. Failure to recognize these concerns may result in noncompliance, protocol violations and research misconduct not being adequately addressed; falsified and/or fabricated methods, data, and results that may be published or used to obtain federal funding; human research subjects being harmed; and/or Public Health Service (PHS) funds not being protected. This data collection is a new request and includes an online survey instrument used with stakeholders holding positions at institutions holding a Federalwide Assurance (FWA) and/or operating an IRB, and is designed to identify barriers in the identification, evaluation, and reporting of potential research misconduct, protocol violations, reportable noncompliance, and unanticipated problems in research that involves human subjects. This data collection is intended to assist ORI and OHRP in developing approaches to improve how to identify and distinguish incidents that are reportable to ORI and OHRP from those that do not require reporting to these offices. This information is also intended to give RIOs, IRBs, human protections administrators, compliance officers, and other institutional officials involved with human subjects' research insight into how they can strengthen their policies and procedures for identifying, evaluating, and/or communicating potential research misconduct and reportable noncompliance and unanticipated problems by identifying gaps, barriers, and areas in which communication and education may need to be enhanced within their institution. <GPOTABLE COLS="06" OPTS="L2,i1" CDEF="s50,12C,12C,12C,12C,12C"> <TTITLE>Annualized Burden Hour Table</TTITLE> <NAME>Sherrette A. Funn,</NAME> Paperwork Reduction Act Reports Clearance Officer, Office of the Secretary. </SIG> </SUPLINF> <FRDOC>[FR Doc. 2024-02649 Filed 2-8-24; 8:45 am]</FRDOC> </NOTICE>