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    An employer (or agent, where applicable) uses this form to petition USCIS for a noncitizen to temporarily enter the United States as an H-1B or H-1B1 nonimmigrant. An employer (or agent, where applicable) also uses this form to request an extension of stay of an H-1B or H-1B1 nonimmigrant worker or to change the status of a beneficiary currently in the United States as a nonimmigrant to H-1B or H-1B1. The form serves the purpose of standardizing requests for H-1B and H-1B1 nonimmigrant workers and ensuring that basic information required for assessing eligibility is provided by the petitioner while requesting that beneficiaries be classified under the H-1B or H-1B1 nonimmigrant employment categories.

    USCIS compiles data from this form to provide information required by Congress annually to assess the effectiveness and utilization of certain nonimmigrant classifications. Data collected on employers petitioning for H-1B beneficiaries is provided to the media, researchers, and the general public via the H-1B Employer Data Hub. (5) An estimate of the total number of respondents and the amount of time estimated for an average respondent to respond.

    The estimated total number of respondents for the information collection Form I-129H1 is 402,034 and the estimated hour burden per response is 4.25 hours. (6) An estimate of the total public burden (in hours) associated with the collection. The total estimated annual hour burden associated with this collection is 1,708,644.50 hours.

    (7) An estimate of the total public burden (in cost) associated with the collection. The estimated total annual cost burden associated with this Start Printed Page 46265collection of information is $207,047,510. Start Signature Dated.

    August 13, 2021. Samantha L. Deshommes, Chief, Regulatory Coordination Division, Office of Policy and Strategy, U.S.

    Citizenship and Immigration Services, Department of Homeland Security. End Signature End Supplemental Information [FR Doc. 2021-17724 Filed 8-17-21.

    8:45 am]BILLING CODE 9111-97-PStart Preamble Health Resources and Services Administration (HRSA), Department of Health and Human Services. Notice. HRSA requests an extension to continue data collection for the Community-Based Workforce for erectile dysfunction treatment Outreach Programs (CBO Programs) (OMB # 0906-0064).

    In compliance with the requirement for opportunity for public comment on proposed data collection projects of the Paperwork Reduction Act of 1995, HRSA announces plans to submit an Information Collection Request (ICR), described below, to the Office of Management and Budget (OMB). Prior to submitting the ICR to OMB, HRSA seeks comments from the public regarding the burden estimate, below, or any other aspect of the ICR. Comments on this ICR should be received no later than October 15, 2021.

    Submit your comments to paperwork@hrsa.gov or by mail to the HRSA Information Collection Clearance Officer, Room 14N136B, 5600 Fishers Lane, Rockville, MD 20857. Start Further Info To request more information on the proposed project or to obtain a copy of the data collection plans and draft instruments, email paperwork@hrsa.gov or call Lisa Wright-Solomon, the HRSA Information Collection Clearance Officer, at (301) 443-1984. End Further Info End Preamble Start Supplemental Information When submitting comments or requesting information, please include the information collection request title for reference.

    Information Collection Request Title. The HRSA Community-Based Outreach Reporting Module, OMB # 0906-0064, Extension. Abstract.

    HRSA requests approval of an extension of the current emergency ICR to continue data collection for the Community-Based Workforce for erectile dysfunction treatment Outreach Programs (CBO Programs), which support nonprofit private or public organizations to establish, expand, and sustain a public health workforce to prevent, prepare for, and respond to erectile dysfunction treatment. This data is needed to comply with requirements to monitor funds distributed under the American Rescue Plan Act of 2021 and in accordance with OMB Memorandum M-21-20. Need and Proposed Use of the Information.

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    117-2), HRSA has awarded nearly $250 million to develop and support a community-based workforce that will engage in locally tailored efforts to build treatment confidence and bolster erectile dysfunction treatment vaccinations in underserved communities. In June and July, under the CBO Programs, HRSA awarded funding to over 140 local and national organizations. These organizations are responsible for educating and assisting individuals in accessing and receiving erectile dysfunction treatment vaccinations.

    This includes activities such as conducting direct face-to-face outreach and other forms of direct outreach to community members to educate them about the treatment, assisting individuals in making a treatment appointment, providing resources to find convenient treatment locations, and assisting individuals with transportation or other needs to get to a vaccination site. The program will address persistent health disparities by offering support and resources to vulnerable and medically underserved communities, including racial and ethnic minority groups and individuals living in areas of high social vulnerability. HRSA is proposing a new data reporting module—the Community-Based treatment Outreach Program Reporting Module—to collect information on CBO Program-funded activities.

    The CBO Program will collect monthly progress report data from funded organizations. This data will be related to the public health workforce, the treatment outreach activities performed by this workforce, and the individuals who received vaccinations by this workforce in a manner that assesses equitable access to treatment services and that the most vulnerable populations and communities are reached. This data will allow HRSA to clearly identify how the funds are being used and monitored throughout the period of performance and to ensure that high-need populations are being reached and vaccinated.

    Responses to some data requirements are only reported during the initial reporting cycle (e.g., the name, location, affiliation, etc. Of the individual supporting community outreach), though respondents may update the data should any of that change during the duration of the reporting period. Likely Respondents.

    Respondents are community outreach workers employed by entities supported by HRSA grant funding over a period of either 6 months (HRSA-21-136) or 12 months (HRSA-21-140). Burden Statement. Burden in this context means the time expended by persons to generate, maintain, retain, Start Printed Page 45740disclose or provide the information requested.

    This includes the time needed to review instructions. To develop, acquire, install, and utilize technology and systems for the purpose of collecting, validating, and verifying information, processing and maintaining information, and disclosing and providing information. To train personnel and to be able to respond to a collection of information.

    To search data sources. To complete and review the collection of information. And to transmit or otherwise disclose the information.

    The total annual burden hours estimated for this ICR are summarized in the table below. Total Estimated Annualized Burden Hours. Form nameNumber of unique organizations funded through the two programsNumber of respondentsNumber of responses per respondentTotal responsesAverage burden per response (in hours)Total burden hoursCommunity outreach worker profile form14 cooperative agreement awards for HRSA-21-136 and 127 grant awards for HRSA-21-136Total number of Community outreach workers deployed through the work of the two programsOne response per respondentReported once across the duration of the programs (the period of performance for HRSA-21-136 is 6 months, and for HRSA-21-140 is 12 months)Sampled response times of approximately 15 minutes per responseTotal hours spent on responses for all funded organizations over a 2-year period. 131 (est.)3,000 (est.)13,0000.27 hours800.

    Form nameNumber of community outreach workersNumber of respondents over the period of the programsNumber of responses per respondentTotal responsesAverage burden per response (in hours)Total burden hourstreatment-site data—outreach to community members formNumber of community outreach workers deployed for 6 months (HRSA-21-136) or 12 months (HRSA-21-140) of supportNumber of community members in contact with community outreach workersOne response per respondent or less (e.g., one response from the audience of a group outreach event)Reported once across the duration of the programs (the period of performance for HRSA-21-136 is 6 months, and for HRSA-21-140 is 12 months)Sampled response times of approximately 6 minutes per responseTotal hours spent on responses for all funded organizations over a 2-year period. 3,000 (est.)4,000,000 (est.)14,000,0000.12 hours466,667.General outreach activities for community members formNumber of community outreach workers deployed for 6 months (HRSA-21-136) or 12 months (HRSA-21-140) of supportNumber of community members in contact with community outreach workersOne response per respondent or less (e.g., one response from the audience of a group outreach event)Reported once across the duration of the programs (the period of performance for HRSA-21-136 is 6 months, and for HRSA-21-140 is 12 months)Sampled response times of approximately 6 minutes per responseTotal hours spent on responses for all funded organizations over a 2-year period. 3,000 (est.)4,000,000 (est.)14,000,0000.12 hours466,667.Grand Total8,003,000 (est.)8,003,000 (est.)934,134. HRSA specifically requests comments on (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. Start Signature Maria G.

    Button, Director, Executive Secretariat. End Signature End Supplemental Information [FR Doc. 2021-17495 Filed 8-13-21.

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    The form serves the purpose of standardizing requests for H-1B and H-1B1 nonimmigrant workers and ensuring that basic information required for assessing eligibility is provided by the petitioner while requesting that beneficiaries be classified under the H-1B or H-1B1 nonimmigrant employment categories. USCIS compiles data from this form to provide information required by Congress annually to assess the effectiveness and utilization of certain nonimmigrant classifications. Data collected on employers petitioning for H-1B beneficiaries is provided to the media, researchers, and the general public via the H-1B Employer Data Hub. (5) An estimate of the total number of respondents and the amount of time estimated for an average respondent to respond.

    The estimated total number of respondents for the information collection Form I-129H1 is 402,034 and the estimated hour burden per response is 4.25 hours. (6) An estimate of the total public burden (in hours) associated with the collection. The total estimated annual hour burden associated with this collection is 1,708,644.50 hours. (7) An estimate of the total public burden (in cost) associated with the collection.

    The estimated total annual cost burden associated with this Start Printed Page 46265collection of information is $207,047,510. Start Signature Dated. August 13, 2021. Samantha L.

    Deshommes, Chief, Regulatory Coordination Division, Office of Policy and Strategy, U.S. Citizenship and Immigration Services, Department of Homeland Security. End Signature End Supplemental Information [FR Doc. 2021-17724 Filed 8-17-21.

    8:45 am]BILLING CODE 9111-97-PStart Preamble Health Resources and Services Administration (HRSA), Department of Health and Human Services. Notice. HRSA requests an extension to continue data collection for the Community-Based Workforce for erectile dysfunction treatment Outreach Programs (CBO Programs) (OMB # 0906-0064). In compliance with the requirement for opportunity for public comment on proposed data collection projects of the Paperwork Reduction Act of 1995, HRSA announces plans to submit an Information Collection Request (ICR), described below, to the Office of Management and Budget (OMB).

    Prior to submitting the ICR to OMB, HRSA seeks comments from the public regarding the burden estimate, below, or any other aspect of the ICR. Comments on this ICR should be received no later than October 15, 2021. Submit your comments to paperwork@hrsa.gov or by mail to the HRSA Information Collection Clearance Officer, Room 14N136B, 5600 Fishers Lane, Rockville, MD 20857. Start Further Info To request more information on the proposed project or to obtain a copy of the data collection plans and draft instruments, email paperwork@hrsa.gov or call Lisa Wright-Solomon, the HRSA Information Collection Clearance Officer, at (301) 443-1984.

    End Further Info End Preamble Start Supplemental Information When submitting comments or requesting information, please include the information collection request title for reference. Information Collection Request Title. The HRSA Community-Based Outreach Reporting Module, OMB # 0906-0064, Extension. Abstract.

    HRSA requests approval of an extension of the current emergency ICR to continue data collection for the Community-Based Workforce for erectile dysfunction treatment Outreach Programs (CBO Programs), which support nonprofit private or public organizations to establish, expand, and sustain a public health workforce to prevent, prepare for, and respond to erectile dysfunction treatment. This data is needed to comply with requirements to monitor funds distributed under the American Rescue Plan Act of 2021 and in accordance with OMB Memorandum M-21-20. Need and Proposed Use of the Information. HRSA is requesting approval from OMB for an extension of the current emergency data collection module to support HRSA's Healthcare Systems Bureau and Office of Planning, Analysis, and Evaluation requirements to monitor and report on funds distributed.

    As part of the American Rescue Plan Act of 2021, signed into law on March 11, 2021 (Pub. L. 117-2), HRSA has awarded nearly $250 million to develop and support a community-based workforce that will engage in locally tailored efforts to build treatment confidence and bolster erectile dysfunction treatment vaccinations in underserved communities. In June and July, under the CBO Programs, HRSA awarded funding to over 140 local and national organizations.

    These organizations are responsible for educating and assisting individuals in accessing and receiving erectile dysfunction treatment vaccinations. This includes activities such as conducting direct face-to-face outreach and other forms of direct outreach to community members to educate them about the treatment, assisting individuals in making a treatment appointment, providing resources to find convenient treatment locations, and assisting individuals with transportation or other needs to get to a vaccination site. The program will address persistent health disparities by offering support and resources to vulnerable and medically underserved communities, including racial and ethnic minority groups and individuals living in areas of high social vulnerability. HRSA is proposing a new data reporting module—the Community-Based treatment Outreach Program Reporting Module—to collect information on CBO Program-funded activities.

    The CBO Program will collect monthly progress report data from funded organizations. This data will be related to the public health workforce, the treatment outreach activities performed by this workforce, and the individuals who received vaccinations by this workforce in a manner that assesses equitable access to treatment services and that the most vulnerable populations and communities are reached. This data will allow HRSA to clearly identify how the funds are being used and monitored throughout the period of performance and to ensure that high-need populations are being reached and vaccinated. Responses to some data requirements are only reported during the initial reporting cycle (e.g., the name, location, affiliation, etc.

    Of the individual supporting community outreach), though respondents may update the data should any of that change during the duration of the reporting period. Likely Respondents. Respondents are community outreach workers employed by entities supported by HRSA grant funding over a period of either 6 months (HRSA-21-136) or 12 months (HRSA-21-140). Burden Statement.

    Burden in this context means the time expended by persons to generate, maintain, retain, Start Printed Page 45740disclose or provide the information requested. This includes the time needed to review instructions. To develop, acquire, install, and utilize technology and systems for the purpose of collecting, validating, and verifying information, processing and maintaining information, and disclosing and providing information. To train personnel and to be able to respond to a collection of information.

    To search data sources. To complete and review the collection of information. And to transmit or otherwise disclose the information. The total annual burden hours estimated for this ICR are summarized in the table below.

    Total Estimated Annualized Burden Hours. Form nameNumber of unique organizations funded through the two programsNumber of respondentsNumber of responses per respondentTotal responsesAverage burden per response (in hours)Total burden hoursCommunity outreach worker profile form14 cooperative agreement awards for HRSA-21-136 and 127 grant awards for HRSA-21-136Total number of Community outreach workers deployed through the work of the two programsOne response per respondentReported once across the duration of the programs (the period of performance for HRSA-21-136 is 6 months, and for HRSA-21-140 is 12 months)Sampled response times of approximately 15 minutes per responseTotal hours spent on responses for all funded organizations over a 2-year period. 131 (est.)3,000 (est.)13,0000.27 hours800. Form nameNumber of community outreach workersNumber of respondents over the period of the programsNumber of responses per respondentTotal responsesAverage burden per response (in hours)Total burden hourstreatment-site data—outreach to community members formNumber of community outreach workers deployed for 6 months (HRSA-21-136) or 12 months (HRSA-21-140) of supportNumber of community members in contact with community outreach workersOne response per respondent or less (e.g., one response from the audience of a group outreach event)Reported once across the duration of the programs (the period of performance for HRSA-21-136 is 6 months, and for HRSA-21-140 is 12 months)Sampled response times of approximately 6 minutes per responseTotal hours spent on responses for all funded organizations over a 2-year period. 3,000 (est.)4,000,000 (est.)14,000,0000.12 hours466,667.General outreach activities for community members formNumber of community outreach workers deployed for 6 months (HRSA-21-136) or 12 months (HRSA-21-140) of supportNumber of community members in contact with community outreach workersOne response per respondent or less (e.g., one response from the audience of a group outreach event)Reported once across the duration of the programs (the period of performance for HRSA-21-136 is 6 months, and for HRSA-21-140 is 12 months)Sampled response times of approximately 6 minutes per responseTotal hours spent on responses for all funded organizations over a 2-year period. 3,000 (est.)4,000,000 (est.)14,000,0000.12 hours466,667.Grand Total8,003,000 (est.)8,003,000 (est.)934,134. HRSA specifically requests comments on (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.

    Start Signature Maria G. Button, Director, Executive Secretariat. End Signature End Supplemental Information [FR Doc. 2021-17495 Filed 8-13-21.

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