Agency Information Collection Activities: Proposed Collection; Comment Request, 36203-36205 [2020-12804]

Download as PDF Federal Register / Vol. 85, No. 115 / Monday, June 15, 2020 / Notices Notice of request for comments regarding an extension to an OMB clearance. ACTION: Under the provisions of the Paperwork Reduction Act, the Regulatory Secretariat Division will be submitting to the Office of Management and Budget (OMB) a request to review and approve an extension of a previously approved information collection requirement regarding the National Contact Center customer evaluation surveys. DATES: Submit comments on or before: July 15, 2020. FOR FURTHER INFORMATION CONTACT: Mr. David Kaufmann, Program Analyst, Office of Technology Transformation Services, via email to david.kaufmann@ gsa.gov, or at 202–357–9661. ADDRESSES: Written comments and recommendations for this 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 Review—Open for Public Comments’’ or by using the search function. SUPPLEMENTARY INFORMATION: SUMMARY: A. Purpose Beth Ann Killoran, Deputy Chief Information Officer. [FR Doc. 2020–12184 Filed 6–12–20; 8:45 am] BILLING CODE 6820–CX–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Agency for Healthcare Research and Quality Agency Information Collection Activities: Proposed Collection; Comment Request Agency for Healthcare Research and Quality, HHS. AGENCY: ACTION: Notice. This notice announces the intention of the Agency for Healthcare Research and Quality (AHRQ) to request that the Office of Management and Budget (OMB) approve the proposed information collection project ‘‘AHRQ Managing Unhealthy Alcohol Use in Primary Care Initiative.’’ This proposed information collection was previously published in the Federal Register on March 30, 2020 and allowed 60 days for public comment. AHRQ did not receive any comments during the aforementioned public comment period. The purpose of this notice is to allow an additional 30 days for public comment. SUMMARY: This information collection will be used to assess the public’s satisfaction with the USA.gov National Contact Center service (formerly the Federal Citizen Information Center’s (FCIC) National Contact Center), to assist in increasing the efficiency in responding to the public’s need for Federal information, and to assess the effectiveness of marketing efforts. B. Annual Reporting Burden jbell on DSKJLSW7X2PROD with NOTICES OBTAINING COPIES OF PROPOSALS: Requesters may obtain a copy of the information collection documents from the GSA Regulatory Secretariat Division (MVCB)by calling 202–501–4755, or emailing GSARegSec@gsa.gov. Please cite OMB Control No. 3090–0278, National Contact Center Customer Evaluation Survey, in all correspondence. The following are estimates of the annual hourly burdens for our surveys based on historical participation in our surveys. (1) Telephone Survey: Respondents: 6000. Responses per Respondent: 1. Annual Responses: 6000. Hours per Response: 0.12. Total Burden Hours: 720. (2) Web Chat Survey: Respondents: 2400. Responses per Respondent: 1. Annual Responses: 2400. Hours Per Response: 0.12. Total Burden Hours: 288. Grand Total Burden Hours: 1008. Comments on this notice must be received by 30 days after date of publication of this notice. DATES: Written comments and recommendations for the 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. ADDRESSES: C. Public Comments FOR FURTHER INFORMATION CONTACT: A 60-day notice was published in the Federal Register at 85 FR 17333 on March 27, 2020. No comments were received. SUPPLEMENTARY INFORMATION: VerDate Sep<11>2014 17:04 Jun 12, 2020 Jkt 250001 Doris Lefkowitz, AHRQ Reports Clearance Officer, (301) 427–1477, or by email at doris.lefkowitz@AHRQ.hhs.gov. PO 00000 Frm 00020 Fmt 4703 Sfmt 4703 36203 Proposed Project AHRQ Managing Unhealthy Alcohol Use in Primary Care Initiative The Affordable Care Act established the Patient-Centered Outcomes Research Trust Fund (PCORTF) and authorized AHRQ to broadly disseminate the research findings published by the Patient-Centered Outcomes Research Institute (PCORI) and other governmentfunded research relevant to comparative clinical effectiveness research. AHRQ’s PCORTF-funded initiative identifies research findings that could significantly improve patient outcomes through broader implementation in clinical practice. Under this initiative, in 2019 AHRQ launched a new initiative, Managing Unhealthy Alcohol Use in Primary Care, in order to promote the uptake of evidence-based practices for unhealthy alcohol use (UAU). As part of this initiative, AHRQ selected six grantees and funded a contractor to support and evaluate the grantees. The grantees will collectively work with more than 700 primary care practices over three years to implement and evaluate strategies to increase the use of evidence-based interventions such as screening for unhealthy alcohol use, brief interventions for adult patients who drink too much, and medication-assisted therapy (MAT) for patients with an alcohol use disorder. The contractor will develop a resource center, convene a technical expert panel, conduct an ongoing environmental scan, support a learning community of grantees, and complete a multisite, mixed methods evaluation. Unhealthy alcohol use, defined as behaviors ranging from risky drinking to alcohol use disorders (AUD), is estimated to be the third leading cause of preventable death in the United States. Between 2006 and 2010, nearly one in ten deaths were alcohol-related. In addition to early mortality, UAU is associated with a host of adverse outcomes, including unintentional injuries and the development or exacerbation of a range of physical and behavioral health conditions. The Centers for Disease Control and Prevention estimates suggest that excessive alcohol consumption costs the United States $249 billion annually. Under the UAU initiative, six AHRQ grantees will work to improve the management of UAU in primary care by disseminating and implementing evidence-based practices for screening and brief intervention, referral to treatment (SBI/RT), and MAT in primary care practices. The multi-site, mixed-methods evaluation will include primary data collection by the evaluator, E:\FR\FM\15JNN1.SGM 15JNN1 36204 Federal Register / Vol. 85, No. 115 / Monday, June 15, 2020 / Notices NORC at the University of Chicago. The evaluation will also include secondary data collected by the six grantee teams working with 750 primary care practices. Collectively the data will allow the evaluator to assess the implementation and impact of the six grants. The project goals, as laid out in the AHRQ request for applications include: • Success of recruitment and retention strategies across all six grantees to engage primary care practices for implementation of SBI/RT and MAT, across the initiative; • Effectiveness of the grantees’ collective dissemination and implementation strategies, and the factors associated with the success and/ or failure of the strategies as it relates to populations, settings and the influence of contextual factors; • Success at the practice level in increasing the number of patients screened, identified, and treated; and • Overall impact on changes in processes or outcomes that can be attributed to the initiative. This study is being conducted pursuant to AHRQ’s statutory authority to broadly disseminate research findings published by the Patient-Centered Outcomes Research Institute and other government-funded research relevant to comparative clinical effectiveness research to physicians, health care providers, and patients. 42 U.S.C 299b– 37. Method of Collection To achieve the goals of the multi-site evaluation (MSE), AHRQ is requesting OMB approval for three years for new data collection by the evaluator. The evaluator’s primary data collection is requested to achieve the goals of the MSE and includes the following data collection activities: Semi-Structured Qualitative Interviews will take place in-person and/or by telephone with key staff from each grantee team (i.e., principal investigator, co-investigator, evaluation lead, practice facilitation/ implementation lead, and project manager) and with clinicians and staff at one primary care practice working with each grantee. Interviews will be conducted annually beginning at the end of Year 1, for a total of three time points per grantee. During Years 1 and 3 the interviews will be conducted by phone, while Year 2 interviews will be collected in-person. The interviews for both grantee teams and primary care practice staff will cover domains such as understanding the practice implementation and changes overtime, methods of supporting practices, barriers and facilitators to implementation, strategies to overcome barriers, and the number and type of staff implementing SBI/RT and MAT. Secondary data collected by grantees and analyzed by the evaluator will include: Aggregated process measure data that will be used to assess whether the number of patients receiving SBI/RT and/or MAT increased at the practice level. Grantees will survey all participating primary care practices at the beginning of the initiative to collect data on basic practice characteristics (e.g., size, ownership, staff, and patient population) that can be used to evaluate relationships between practice characteristics and the number of patients receiving SBI/RT and/or MAT. Grantees will also collect quantitative information about the number, duration, and function of contact between practice facilitators and primary care practices to evaluate the relationship between duration, frequency, and type of practice facilitator-practice engagement, and the number of patients screened, receiving brief intervention, and/or treated for UAU. The practice facilitators will collect data to track changes in practices over time and facilitate an overall assessment of what activities the practice is conducting to identify and manage UAU. Estimated Annual Respondent Burden Exhibit 1 shows the estimated annualized burden hours for the respondents’ time to complete the semistructured Key Informant Interviews. For the three-year clearance period, the estimated annualized burden hours for the interviews are 60. EXHIBIT 1 Number of respondents Data collection activity Number of responses per respondent Hours per response Total burden hours Semi-Structured Interviews .............................................................................. 60 1 1.0 60 Total .......................................................................................................... 60 ........................ ........................ 60 Exhibit 2 shows the estimated annualized cost burden based on the respondents’ time to complete the Key Informant Interviews. The total annualized cost burden is estimated to be $6,109. EXHIBIT 2—ESTIMATED ANNUALIZED COST BURDEN Number of respondents jbell on DSKJLSW7X2PROD with NOTICES Form name Total burden hours Average hourly wage rate * Total cost burden Semi-Structured Interviews .............................................................................. 60 60 a $101.82 $6,109 Total .......................................................................................................... 60 60 ........................ 6,109 * National Compensation Survey: Occupational wages in the United States May 2018 ‘‘U.S. Department of Labor, Bureau of Labor Statistics’’: https://www.bls.gov/oes/current/oes_stru.htm. a Based on the mean wages for 29–1062 Family and General Practitioners. Request for Comments In accordance with the Paperwork Reduction Act, comments on AHRQ’s VerDate Sep<11>2014 17:04 Jun 12, 2020 Jkt 250001 information collection are requested with regard to any of the following: (a) Whether the proposed collection of PO 00000 Frm 00021 Fmt 4703 Sfmt 4703 information is necessary for the proper performance of AHRQ’s health care research and health care information E:\FR\FM\15JNN1.SGM 15JNN1 Federal Register / Vol. 85, No. 115 / Monday, June 15, 2020 / Notices dissemination functions, including whether the information will have practical utility; (b) the accuracy of AHRQ’s estimate of burden (including hours and costs) of the proposed collection(s) of information; (c) ways to enhance the quality, utility and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information upon the respondents, including the use of automated collection techniques or other forms of information technology. Comments submitted in response to this notice will be summarized and included in the Agency’s subsequent request for OMB approval of the proposed information collection. All comments will become a matter of public record. Dated: June 9, 2020. Virginia L. Mackay-Smith, Associate Director. BILLING CODE 4160–90–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60 Day-20–1161; Docket No. CDC–2020– 0068] 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 and/or continuing information collection, as required by the Paperwork Reduction Act of 1995. This notice invites comment on a proposed information collection project titled ‘‘Evaluation of Enhancing HIV Prevention Communication and Mobilization Efforts through Strategic Partnerships.’’ This collection is designed to assess the extent to which partnership activities meet the overarching goals for dissemination, communication, and implementation of national engagement efforts in support of the U.S. Department of Health and Human Services’ Ending the HIV Epidemic. jbell on DSKJLSW7X2PROD with NOTICES VerDate Sep<11>2014 17:04 Jun 12, 2020 Jkt 250001 Please note: Submit all comments through the Federal eRulemaking portal (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 instruments, contact Jeffrey M. Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS– D74, Atlanta, Georgia 30329; phone: 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 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; FOR FURTHER INFORMATION CONTACT: [FR Doc. 2020–12804 Filed 6–12–20; 8:45 am] SUMMARY: CDC must receive written comments on or before August 14, 2020. ADDRESSES: You may submit comments, identified by Docket No. CDC–2020– 0068 by any of the following methods: • Federal eRulemaking Portal: 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–D74, Atlanta, Georgia 30329. Instructions: All submissions received must include the agency name and Docket Number. CDC will post, without change, all relevant comments to Regulations.gov. DATES: PO 00000 Frm 00022 Fmt 4703 Sfmt 4703 36205 3. Enhance the quality, utility, and clarity of the information to be collected; and 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. 5. Assess information collection costs. Proposed Project Evaluation of Enhancing HIV Prevention Communication and Mobilization Efforts through Strategic Partnerships (OMB Control No. 0920– 1161)—Reinstatement without Change— National Center for HIV/AIDS, Viral Hepatitis, STD and TB Prevention (NCHHSTP), Centers for Disease Control and Prevention (CDC). Background and Brief Description To address the HIV epidemic in the U.S., the Department of Health and Human Services launched Ending the HIV Epidemic: A Plan for America, which is a cross-agency initiative aiming to reduce new HIV infections in the U.S. by 90% by 2030. CDC’s Let’s Stop HIV Together campaign (formerly known as Act Against AIDS) is part of the national Ending the HIV Epidemic initiative, and includes resources aimed at reducing HIV stigma and promoting testing, prevention, and treatment across the HIV care continuum. Within this context, CDC’s Division of HIV/AIDS Prevention (DHAP) has and will continue implementing various partnership activities to increase HIV awareness among the general public, reduce new HIV infections among disproportionately impacted populations, and improve health outcomes for people living with HIV/ AIDS in the US and its territories. DHAP partners will be funded under to (1) support the dissemination of Together campaign materials, messaging, and other CDC resources that support HIV prevention and (2) implement national engagement efforts focusing on HIV prevention and awareness. Partners represent civic/ social, media, and LGBT-focused organizations. In addition, DHAP will continue to engage and support the private sector in promoting HIV education, awareness, and policies in the workplace. This may take the form of encouraging businesses to implement HIV/AIDS policies and education programs in the workplace with the overarching goal of increasing public E:\FR\FM\15JNN1.SGM 15JNN1

Agencies

[Federal Register Volume 85, Number 115 (Monday, June 15, 2020)]
[Notices]
[Pages 36203-36205]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-12804]


=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Agency for Healthcare Research and Quality


Agency Information Collection Activities: Proposed Collection; 
Comment Request

AGENCY: Agency for Healthcare Research and Quality, HHS.

ACTION: Notice.

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

SUMMARY: This notice announces the intention of the Agency for 
Healthcare Research and Quality (AHRQ) to request that the Office of 
Management and Budget (OMB) approve the proposed information collection 
project ``AHRQ Managing Unhealthy Alcohol Use in Primary Care 
Initiative.'' This proposed information collection was previously 
published in the Federal Register on March 30, 2020 and allowed 60 days 
for public comment. AHRQ did not receive any comments during the 
aforementioned public comment period. The purpose of this notice is to 
allow an additional 30 days for public comment.

DATES: Comments on this notice must be received by 30 days after date 
of publication of this notice.

ADDRESSES: Written comments and recommendations for the 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.

FOR FURTHER INFORMATION CONTACT: Doris Lefkowitz, AHRQ Reports 
Clearance Officer, (301) 427-1477, or by email at 
[email protected].

SUPPLEMENTARY INFORMATION:

Proposed Project

AHRQ Managing Unhealthy Alcohol Use in Primary Care Initiative

    The Affordable Care Act established the Patient-Centered Outcomes 
Research Trust Fund (PCORTF) and authorized AHRQ to broadly disseminate 
the research findings published by the Patient-Centered Outcomes 
Research Institute (PCORI) and other government-funded research 
relevant to comparative clinical effectiveness research. AHRQ's PCORTF-
funded initiative identifies research findings that could significantly 
improve patient outcomes through broader implementation in clinical 
practice. Under this initiative, in 2019 AHRQ launched a new 
initiative, Managing Unhealthy Alcohol Use in Primary Care, in order to 
promote the uptake of evidence-based practices for unhealthy alcohol 
use (UAU). As part of this initiative, AHRQ selected six grantees and 
funded a contractor to support and evaluate the grantees. The grantees 
will collectively work with more than 700 primary care practices over 
three years to implement and evaluate strategies to increase the use of 
evidence-based interventions such as screening for unhealthy alcohol 
use, brief interventions for adult patients who drink too much, and 
medication-assisted therapy (MAT) for patients with an alcohol use 
disorder. The contractor will develop a resource center, convene a 
technical expert panel, conduct an ongoing environmental scan, support 
a learning community of grantees, and complete a multisite, mixed 
methods evaluation.
    Unhealthy alcohol use, defined as behaviors ranging from risky 
drinking to alcohol use disorders (AUD), is estimated to be the third 
leading cause of preventable death in the United States. Between 2006 
and 2010, nearly one in ten deaths were alcohol-related. In addition to 
early mortality, UAU is associated with a host of adverse outcomes, 
including unintentional injuries and the development or exacerbation of 
a range of physical and behavioral health conditions. The Centers for 
Disease Control and Prevention estimates suggest that excessive alcohol 
consumption costs the United States $249 billion annually.
    Under the UAU initiative, six AHRQ grantees will work to improve 
the management of UAU in primary care by disseminating and implementing 
evidence-based practices for screening and brief intervention, referral 
to treatment (SBI/RT), and MAT in primary care practices. The multi-
site, mixed-methods evaluation will include primary data collection by 
the evaluator,

[[Page 36204]]

NORC at the University of Chicago. The evaluation will also include 
secondary data collected by the six grantee teams working with 750 
primary care practices. Collectively the data will allow the evaluator 
to assess the implementation and impact of the six grants.
    The project goals, as laid out in the AHRQ request for applications 
include:
     Success of recruitment and retention strategies across all 
six grantees to engage primary care practices for implementation of 
SBI/RT and MAT, across the initiative;
     Effectiveness of the grantees' collective dissemination 
and implementation strategies, and the factors associated with the 
success and/or failure of the strategies as it relates to populations, 
settings and the influence of contextual factors;
     Success at the practice level in increasing the number of 
patients screened, identified, and treated; and
     Overall impact on changes in processes or outcomes that 
can be attributed to the initiative.
    This study is being conducted pursuant to AHRQ's statutory 
authority to broadly disseminate research findings published by the 
Patient-Centered Outcomes Research Institute and other government-
funded research relevant to comparative clinical effectiveness research 
to physicians, health care providers, and patients. 42 U.S.C 299b-37.

Method of Collection

    To achieve the goals of the multi-site evaluation (MSE), AHRQ is 
requesting OMB approval for three years for new data collection by the 
evaluator. The evaluator's primary data collection is requested to 
achieve the goals of the MSE and includes the following data collection 
activities:
    Semi-Structured Qualitative Interviews will take place in-person 
and/or by telephone with key staff from each grantee team (i.e., 
principal investigator, co-investigator, evaluation lead, practice 
facilitation/implementation lead, and project manager) and with 
clinicians and staff at one primary care practice working with each 
grantee. Interviews will be conducted annually beginning at the end of 
Year 1, for a total of three time points per grantee. During Years 1 
and 3 the interviews will be conducted by phone, while Year 2 
interviews will be collected in-person. The interviews for both grantee 
teams and primary care practice staff will cover domains such as 
understanding the practice implementation and changes overtime, methods 
of supporting practices, barriers and facilitators to implementation, 
strategies to overcome barriers, and the number and type of staff 
implementing SBI/RT and MAT.
    Secondary data collected by grantees and analyzed by the evaluator 
will include:
    Aggregated process measure data that will be used to assess whether 
the number of patients receiving SBI/RT and/or MAT increased at the 
practice level. Grantees will survey all participating primary care 
practices at the beginning of the initiative to collect data on basic 
practice characteristics (e.g., size, ownership, staff, and patient 
population) that can be used to evaluate relationships between practice 
characteristics and the number of patients receiving SBI/RT and/or MAT. 
Grantees will also collect quantitative information about the number, 
duration, and function of contact between practice facilitators and 
primary care practices to evaluate the relationship between duration, 
frequency, and type of practice facilitator-practice engagement, and 
the number of patients screened, receiving brief intervention, and/or 
treated for UAU. The practice facilitators will collect data to track 
changes in practices over time and facilitate an overall assessment of 
what activities the practice is conducting to identify and manage UAU.

Estimated Annual Respondent Burden

    Exhibit 1 shows the estimated annualized burden hours for the 
respondents' time to complete the semi-structured Key Informant 
Interviews. For the three-year clearance period, the estimated 
annualized burden hours for the interviews are 60.

                                                    Exhibit 1
----------------------------------------------------------------------------------------------------------------
                                                                     Number of
            Data collection activity                 Number of     responses per     Hours per     Total burden
                                                    respondents     respondent       response          hours
----------------------------------------------------------------------------------------------------------------
Semi-Structured Interviews......................              60               1             1.0              60
                                                 ---------------------------------------------------------------
    Total.......................................              60  ..............  ..............              60
----------------------------------------------------------------------------------------------------------------

    Exhibit 2 shows the estimated annualized cost burden based on the 
respondents' time to complete the Key Informant Interviews. The total 
annualized cost burden is estimated to be $6,109.

                                   Exhibit 2--Estimated Annualized Cost Burden
----------------------------------------------------------------------------------------------------------------
                                                     Number of     Total burden   Average hourly    Total cost
                    Form name                       respondents        hours        wage rate *       burden
----------------------------------------------------------------------------------------------------------------
Semi-Structured Interviews......................              60              60     \a\ $101.82          $6,109
                                                 ---------------------------------------------------------------
    Total.......................................              60              60  ..............           6,109
----------------------------------------------------------------------------------------------------------------
* National Compensation Survey: Occupational wages in the United States May 2018 ``U.S. Department of Labor,
  Bureau of Labor Statistics'': https://www.bls.gov/oes/current/oes_stru.htm.
\a\ Based on the mean wages for 29-1062 Family and General Practitioners.

Request for Comments

    In accordance with the Paperwork Reduction Act, comments on AHRQ's 
information collection are requested with regard to any of the 
following: (a) Whether the proposed collection of information is 
necessary for the proper performance of AHRQ's health care research and 
health care information

[[Page 36205]]

dissemination functions, including whether the information will have 
practical utility; (b) the accuracy of AHRQ's estimate of burden 
(including hours and costs) of the proposed collection(s) of 
information; (c) ways to enhance the quality, utility and clarity of 
the information to be collected; and (d) ways to minimize the burden of 
the collection of information upon the respondents, including the use 
of automated collection techniques or other forms of information 
technology.
    Comments submitted in response to this notice will be summarized 
and included in the Agency's subsequent request for OMB approval of the 
proposed information collection. All comments will become a matter of 
public record.

    Dated: June 9, 2020.
Virginia L. Mackay-Smith,
Associate Director.
[FR Doc. 2020-12804 Filed 6-12-20; 8:45 am]
BILLING CODE 4160-90-P