Proposed Collection; 60-Day Comment Request Data and Specimen Hub (DASH) (Eunice Kennedy Shriver National Institute of Child Health and Human Development), 3160-3162 [2021-00636]

Download as PDF khammond on DSKJM1Z7X2PROD with NOTICES 3160 Federal Register / Vol. 86, No. 9 / Thursday, January 14, 2021 / Notices www.minorityhealth.hhs.gov. Information about ACMH activities can be found on the OMH website under the heading About OMH, Committees and Workgroups. DATES: The ACMH meeting will be held on Friday, January 29, 2021, from 1:30 p.m. to 2:00 p.m. ET. If the Committee completes its work before 2:00 p.m., the meeting will end early. ADDRESSES: The meeting will be held virtually and will be accessible by webcast. FOR FURTHER INFORMATION CONTACT: Samuel Wu, Designated Federal Officer, Advisory Committee on Minority Health, Office of Minority Health, Department of Health and Human Services, Tower Building, 1101 Wootton Parkway, Suite 100, Rockville, Maryland 20852. Phone: 240–453–6173; email: OMH-ACMH@hhs.gov. SUPPLEMENTARY INFORMATION: In accordance with Public Law 105–392, the ACMH was established to provide advice to the Deputy Assistant Secretary for Minority Health on improving the health of each racial and ethnic minority group and on the development of goals and specific program activities of the OMH. The purpose of the January 2021 ACMH meeting is to finalize recommendations for improving access to and utilization of clinical preventive services among racial and ethnic minority populations. The recommendations will be given to the Deputy Assistant Secretary for Minority Health to inform efforts for removing barriers to achieving health equity. The meeting is open to the public. Any individual who wishes to attend the meeting must register by sending an email to OMH-ACMH@hhs.gov by 5:00 p.m. ET on January 28, 2021. Each registrant should provide name, affiliation, phone number, and email address. Registrants will receive webcast access information via email. Individuals who plan to attend and need special assistance, such as sign language interpretation or other reasonable accommodations, should contact OMH-ACMH@hhs.gov and reference this meeting. Requests for special accommodations should be made at least ten (10) business days prior to the meeting. Members of the public will have an opportunity to provide comments at the meeting. Public comments will be limited to two minutes per speaker during the time allotted. Individuals who would like to submit written statements should email OMH-ACMH@ hhs.gov at least five (5) business days prior to the meeting. VerDate Sep<11>2014 20:43 Jan 13, 2021 Jkt 253001 Dated: January 8, 2021. Tyeshia M. Roberson, Program Analyst, Office of Federal Advisory Committee Policy. Any members of the public who wish to distribute electronic or printed material(s) related to this meeting’s topic to ACMH members should email the Designated Federal Officer at OMHACMH@hhs.gov. The material should be received by the Designated Federal Officer at least five (5) business days prior to the meeting. [FR Doc. 2021–00576 Filed 1–13–21; 8:45 am] Dated: January 11, 2021. Samuel Wu, Designated Federal Officer, Advisory Committee on Minority Health. National Institutes of Health BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES BILLING CODE 4150–29–P Proposed Collection; 60-Day Comment Request Data and Specimen Hub (DASH) (Eunice Kennedy Shriver National Institute of Child Health and Human Development) DEPARTMENT OF HEALTH AND HUMAN SERVICES AGENCY: National Institutes of Health ACTION: National Institute on Drug Abuse; Notice of Closed Meeting SUMMARY: [FR Doc. 2021–00660 Filed 1–13–21; 8:45 am] Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended, notice is hereby given of the following meeting. The meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: National Institute on Drug Abuse Special Emphasis Panel; Interventions to Prevent Electronic Nicotine Delivery Systems (ENDS) Use Among Adolescents (R01—Clinical Trial Optional). Date: March 10, 2021. Time: 9:00 a.m. to 6:00 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, National Institute on Drug Abuse, 301 North Stonestreet Avenue, Bethesda, MD 20892 (Virtual Meeting). Contact Person: Yvonne Owens Ferguson, Ph.D., Scientific Review Officer, Office of Extramural Policy and Review, Division of Extramural Research, National Institute on Drug Abuse, NIH, 301 North Stonestreet Avenue, MSC 6021, Bethesda, MD 20892, (301) 402–7371, yvonne.ferguson@nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.277, Drug Abuse Scientist Development Award for Clinicians, Scientist Development Awards, and Research Scientist Awards; 93.278, Drug Abuse National Research Service Awards for Research Training; 93.279, Drug Abuse and Addiction Research Programs, National Institutes of Health, HHS) PO 00000 Frm 00052 Fmt 4703 Sfmt 4703 National Institutes of Health, HHS. Notice. In compliance with the requirement of the Paperwork Reduction Act of 1995 to provide opportunity for public comment on proposed data collection projects, the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), the National Institutes of Health will publish periodic summaries of propose projects to be submitted to the Office of Management and Budget (OMB) for review and approval. DATES: Comments regarding this information collection are best assured of having their full effect if received within 60 days of the date of this publication. FOR FURTHER INFORMATION CONTACT: To obtain a copy of the data collection plans and instruments, submit comments in writing, or request more information on the proposed project, contact: Regina Bures, Ph.D., Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health, 6710B Rockledge Drive, Room 2160, Bethesda, MD 20817, or call non-tollfree number (301) 496–9485 or Email your request, including your address to: NICHD.DASH@mail.nih.gov. Formal requests for additional plans and instruments must be requested in writing. SUPPLEMENTARY INFORMATION: Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995 requires: Written comments and/or suggestions from the public and affected agencies are invited to address one or more of the following points: (1) Whether the proposed collection of information is necessary for the proper performance of the function of the agency, including whether the information will have E:\FR\FM\14JAN1.SGM 14JAN1 3161 Federal Register / Vol. 86, No. 9 / Thursday, January 14, 2021 / Notices practical utility; (2) 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) Ways to enhance the quality, utility, and clarity of the information to be collected; and (4) Ways to minimize the burden of the collection of information on those who are to respond, including the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology. Proposed Collection Title: Data and Specimen Hub (DASH)-0925–0744 expiration date 01/31/2022, REVISION, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH). Need and Use of Information Collection: This is a request to revise the previously approved submission (OMB number: 0925–0744) to add the collection of additional information from Users who will submit information to NICHD Data and Specimen Hub (DASH) about studies, and data collections stored in publicly accessible external archives—a process hereinafter referred to as ‘cataloging’ in DASH. DASH has been established by NICHD as a data sharing mechanism for biomedical research investigators. It serves as a centralized resource for investigators to share and access deidentified study data from studies funded by NICHD. DASH also serves as a portal for requesting biospecimens from selected DASH studies. NICHD also supports other public archives, data collections, and resources, such as Data Sharing for Demographic Research (DSDR), NICHD/ DIPHR Biospecimen Repository Access and Data Sharing (BRADS), the Down Syndrome Registry (DS-Connect), Zebrafish Information Network (ZFIN), etc. In addition to these NICHD-funded public archives, many collaborative studies funded through NICHD are dispersed across other National Institutes of Health (NIH) designated archives, including the National Heart, Lung, and Blood Institute (NHLBI) Biologic Specimen and Data Repository information about the studies and data collections without creating an account. Users who wish to submit studies or request data stored in DASH, and/or request biospecimens (stored in NICHD contracted Biorepository) must register for an account; Users who wish to submit a study catalog and/or data collection catalog must also register for an account. Information will be collected from those wishing to create an account, sufficient to identify them as unique Users. Those submitting or requesting data and/or biospecimens will be required to provide additional supporting information to ensure proper use and security of NICHD DASH study data and biospecimens. The information collected is limited to the essential data required to ensure the management of Users in NICHD DASH is efficient and the sharing of data and biospecimens among investigators is effective. The primary uses of the information collected from Uses by NICHD will be to: • Communicate with the Users regarding data submission, study catalog submission, data collection catalog submission, data requests and biospecimen requests; • Monitor data submissions, study catalog submission, data collection catalog submission, data requests and biospecimen requests; • Notify interested Users of updates to data and biospecimen inventories stored in NICHD DASH; and • Help NICHD understand the use of NICHD DASH study data and biospecimen inventories by the research community. All the data collected from use of NICHD DASH except for information provided in the annual progress reports are for the purposes of internal administrative management of NICHD DASH. Information gathered through the annual progress reports may be used in publications describing performance of the DASH system. OMB approval is requested for 3 years. There are no costs to respondents other than their time. The total estimated annualized burden hours are 211. Information Coordinating Center (BioLINCC), and other NIH-wide repositories, such as the Database of Genotypes and Phenotypes (dbGaP). In an effort to link these data resources and increase the visibility of NICHD-funded studies and data collections, DASH will enable Users to catalog studies and data collections stored in other external archives to facilitate their discovery through DASH. Users submitting studies or data collections for cataloging in DASH will provide descriptive information about the study required to populate the Study Overview Page in DASH. This cataloging process closely mirrors the existing study data submission process in DASH; however, no study documentation or data will be uploaded to DASH. Requesters will be directed to the external archive via a URL link to obtain access to the data stored in the external archives and resources. The potential for public benefit to be achieved through sharing study data and/or biospecimen inventories through DASH for secondary analysis is significant. Additionally, the ability to centralize information regarding where to find, and how to access, studies, and data collections funded by NICHD stored across various public archives (i.e., cataloged studies and data collections) further helps to promote information discovery and reuse of data. NICHD DASH supports NICHD’s mission to ensure that every person is born healthy and wanted; that women suffer no harmful effects from reproductive processes; that all children have the chance to achieve their full potential for healthy and productive lives, free from disease or disability; and to ensure the health, productivity, independence, and well-being of all people through optimal rehabilitation. Study data and biospecimen sharing and reuse will promote testing of new hypotheses from data and biospecimens already collected, facilitate transdisciplinary collaboration, accelerate scientific findings and enable NICHD to maximize the return on its investments in research. Anyone can access NICHD DASH to browse and view descriptive khammond on DSKJM1Z7X2PROD with NOTICES ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Type of form User Registration ............................................................................................. Data and Biospecimen Inventory Submissions ............................................... Study Catalog Submission .............................................................................. Data Collection Catalog Submission ............................................................... Data Request ................................................................................................... VerDate Sep<11>2014 20:43 Jan 13, 2021 Jkt 253001 PO 00000 Frm 00053 Fmt 4703 Sfmt 4703 Frequency of response per respondent 200 36 10 6 60 E:\FR\FM\14JAN1.SGM 1 1 1 1 1 14JAN1 Average time per response (in hours) 5/60 2 30/60 15/60 1 Total annual burden hour 17 72 5 2 60 3162 Federal Register / Vol. 86, No. 9 / Thursday, January 14, 2021 / Notices ESTIMATED ANNUALIZED BURDEN HOURS—Continued Number of respondents Type of form Frequency of response per respondent Average time per response (in hours) Total annual burden hour Biospecimen Request ...................................................................................... Data Use Annual Progress Report .................................................................. Biospecimen Use Annual Progress Report ..................................................... Institutional Certification Template .................................................................. 36 60 36 36 1 1 1 1 1 10/60 10/60 5/60 36 10 6 3 Total .......................................................................................................... 200 200 ........................ 211 Dated: January 5, 2021. Jennifer M. Guimond, Project Clearance Liaison, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health. [FR Doc. 2021–00636 Filed 1–13–21; 8:45 am] Fishers Lane, Room 3G62A, Rockville, MD 20852, (240) 669–5069, lrust@niaid.nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.855, Allergy, Immunology, and Transplantation Research; 93.856, Microbiology and Infectious Diseases Research, National Institutes of Health, HHS) Dated: January 8, 2021. Tyeshia M. Roberson, Program Analyst, Office of Federal Advisory Committee Policy. BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES [FR Doc. 2021–00577 Filed 1–13–21; 8:45 am] BILLING CODE 4140–01–P National Institutes of Health National Institute of Allergy and Infectious Diseases; Notice of Closed Meeting DEPARTMENT OF HEALTH AND HUMAN SERVICES North Stonestreet Avenue, MSC 6021, Bethesda, MD 20892, (301) 594–9460, Soyoun.cho@nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.277, Drug Abuse Scientist Development Award for Clinicians, Scientist Development Awards, and Research Scientist Awards; 93.278, Drug Abuse National Research Service Awards for Research Training; 93.279, Drug Abuse and Addiction Research Programs, National Institutes of Health, HHS) Dated: January 8, 2021. Tyeshia M. Roberson, Program Analyst, Office of Federal Advisory Committee Policy. [FR Doc. 2021–00575 Filed 1–13–21; 8:45 am] BILLING CODE 4140–01–P National Institutes of Health khammond on DSKJM1Z7X2PROD with NOTICES Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended, notice is hereby given of the following meeting. The meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The contract proposals and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the contract proposals, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: National Institute of Allergy and Infectious Diseases Special Emphasis Panel; A Solicitation of the National Institutes of Health (NIH) and the Centers for Disease Control and Prevention (CDC) for Small Business Innovation Research (SBIR) Contract Proposals (N01), Topic 100. Date: February 2, 2021. Time: 11:00 a.m. to 4:00 p.m. Agenda: To review and evaluate contract proposals. Place: National Institute of Allergy and Infectious Diseases, National Institutes of Health, 5601 Fishers Lane, Room 3G62A, Rockville, MD 20892 (Virtual Meeting). Contact Person: Lynn Rust, Ph.D., Scientific Review Officer, Scientific Review Program, Division of Extramural Activities, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 5601 VerDate Sep<11>2014 20:43 Jan 13, 2021 Jkt 253001 National Institute on Drug Abuse; Notice of Closed Meeting Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended, notice is hereby given of the following meeting. The meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: National Institute on Drug Abuse Special Emphasis Panel; Exploring Epigenomic or Non-Coding RNA Regulation in the Development, Maintenance, or Treatment of Chronic Pain (R61/R33 Clinical Trial Optional). Date: February 22, 2021. Time: 2:00 p.m. to 4:00 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health National Institute on Drug Abuse 301 North Stonestreet Avenue Bethesda, MD 20892 (Virtual Meeting). Contact Person: Soyoun Cho, Ph.D., Scientific Review Officer, Scientific Review Branch, Division of Extramural Research, National Institute on Drug Abuse, NIH, 301 PO 00000 Frm 00054 Fmt 4703 Sfmt 4703 DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute of Nursing Research; Notice of Closed Meetings Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended, notice is hereby given of the following meetings. The meetings will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: National Institute of Nursing Research Special Emphasis Panel; Modular Budget Research Project Grant for NIH Nurse Scientist Scholars. Date: February 5, 2021. Time: 10:00 a.m. to 3:00 p.m. Agenda: To review and evaluate grant applications. Place: National Institute of Nursing Research, National Institutes of Health, 6701 Democracy Boulevard, Bethesda, MD 20892 (Virtual Meeting). E:\FR\FM\14JAN1.SGM 14JAN1

Agencies

[Federal Register Volume 86, Number 9 (Thursday, January 14, 2021)]
[Notices]
[Pages 3160-3162]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-00636]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Proposed Collection; 60-Day Comment Request Data and Specimen Hub 
(DASH) (Eunice Kennedy Shriver National Institute of Child Health and 
Human Development)

AGENCY: National Institutes of Health, HHS.

ACTION: Notice.

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

SUMMARY: In compliance with the requirement of the Paperwork Reduction 
Act of 1995 to provide opportunity for public comment on proposed data 
collection projects, the Eunice Kennedy Shriver National Institute of 
Child Health and Human Development (NICHD), the National Institutes of 
Health will publish periodic summaries of propose projects to be 
submitted to the Office of Management and Budget (OMB) for review and 
approval.

DATES: Comments regarding this information collection are best assured 
of having their full effect if received within 60 days of the date of 
this publication.

FOR FURTHER INFORMATION CONTACT: To obtain a copy of the data 
collection plans and instruments, submit comments in writing, or 
request more information on the proposed project, contact: Regina 
Bures, Ph.D., Eunice Kennedy Shriver National Institute of Child Health 
and Human Development (NICHD), National Institutes of Health, 6710B 
Rockledge Drive, Room 2160, Bethesda, MD 20817, or call non-toll-free 
number (301) 496-9485 or Email your request, including your address to: 
[email protected]. Formal requests for additional plans and 
instruments must be requested in writing.

SUPPLEMENTARY INFORMATION: Section 3506(c)(2)(A) of the Paperwork 
Reduction Act of 1995 requires: Written comments and/or suggestions 
from the public and affected agencies are invited to address one or 
more of the following points: (1) Whether the proposed collection of 
information is necessary for the proper performance of the function of 
the agency, including whether the information will have

[[Page 3161]]

practical utility; (2) 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) Ways to enhance 
the quality, utility, and clarity of the information to be collected; 
and (4) Ways to minimize the burden of the collection of information on 
those who are to respond, including the use of appropriate automated, 
electronic, mechanical, or other technological collection techniques or 
other forms of information technology.
    Proposed Collection Title: Data and Specimen Hub (DASH)-0925-0744 
expiration date 01/31/2022, REVISION, Eunice Kennedy Shriver National 
Institute of Child Health and Human Development (NICHD), National 
Institutes of Health (NIH).
    Need and Use of Information Collection: This is a request to revise 
the previously approved submission (OMB number: 0925-0744) to add the 
collection of additional information from Users who will submit 
information to NICHD Data and Specimen Hub (DASH) about studies, and 
data collections stored in publicly accessible external archives--a 
process hereinafter referred to as `cataloging' in DASH.
    DASH has been established by NICHD as a data sharing mechanism for 
biomedical research investigators. It serves as a centralized resource 
for investigators to share and access de-identified study data from 
studies funded by NICHD. DASH also serves as a portal for requesting 
biospecimens from selected DASH studies.
    NICHD also supports other public archives, data collections, and 
resources, such as Data Sharing for Demographic Research (DSDR), NICHD/
DIPHR Biospecimen Repository Access and Data Sharing (BRADS), the Down 
Syndrome Registry (DS-Connect), Zebrafish Information Network (ZFIN), 
etc. In addition to these NICHD-funded public archives, many 
collaborative studies funded through NICHD are dispersed across other 
National Institutes of Health (NIH) designated archives, including the 
National Heart, Lung, and Blood Institute (NHLBI) Biologic Specimen and 
Data Repository Information Coordinating Center (BioLINCC), and other 
NIH-wide repositories, such as the Database of Genotypes and Phenotypes 
(dbGaP).
    In an effort to link these data resources and increase the 
visibility of NICHD-funded studies and data collections, DASH will 
enable Users to catalog studies and data collections stored in other 
external archives to facilitate their discovery through DASH. Users 
submitting studies or data collections for cataloging in DASH will 
provide descriptive information about the study required to populate 
the Study Overview Page in DASH. This cataloging process closely 
mirrors the existing study data submission process in DASH; however, no 
study documentation or data will be uploaded to DASH. Requesters will 
be directed to the external archive via a URL link to obtain access to 
the data stored in the external archives and resources.
    The potential for public benefit to be achieved through sharing 
study data and/or biospecimen inventories through DASH for secondary 
analysis is significant. Additionally, the ability to centralize 
information regarding where to find, and how to access, studies, and 
data collections funded by NICHD stored across various public archives 
(i.e., cataloged studies and data collections) further helps to promote 
information discovery and reuse of data. NICHD DASH supports NICHD's 
mission to ensure that every person is born healthy and wanted; that 
women suffer no harmful effects from reproductive processes; that all 
children have the chance to achieve their full potential for healthy 
and productive lives, free from disease or disability; and to ensure 
the health, productivity, independence, and well-being of all people 
through optimal rehabilitation. Study data and biospecimen sharing and 
reuse will promote testing of new hypotheses from data and biospecimens 
already collected, facilitate trans-disciplinary collaboration, 
accelerate scientific findings and enable NICHD to maximize the return 
on its investments in research.
    Anyone can access NICHD DASH to browse and view descriptive 
information about the studies and data collections without creating an 
account. Users who wish to submit studies or request data stored in 
DASH, and/or request biospecimens (stored in NICHD contracted 
Biorepository) must register for an account; Users who wish to submit a 
study catalog and/or data collection catalog must also register for an 
account.
    Information will be collected from those wishing to create an 
account, sufficient to identify them as unique Users. Those submitting 
or requesting data and/or biospecimens will be required to provide 
additional supporting information to ensure proper use and security of 
NICHD DASH study data and biospecimens. The information collected is 
limited to the essential data required to ensure the management of 
Users in NICHD DASH is efficient and the sharing of data and 
biospecimens among investigators is effective. The primary uses of the 
information collected from Uses by NICHD will be to:
     Communicate with the Users regarding data submission, 
study catalog submission, data collection catalog submission, data 
requests and biospecimen requests;
     Monitor data submissions, study catalog submission, data 
collection catalog submission, data requests and biospecimen requests;
     Notify interested Users of updates to data and biospecimen 
inventories stored in NICHD DASH; and
     Help NICHD understand the use of NICHD DASH study data and 
biospecimen inventories by the research community.
    All the data collected from use of NICHD DASH except for 
information provided in the annual progress reports are for the 
purposes of internal administrative management of NICHD DASH. 
Information gathered through the annual progress reports may be used in 
publications describing performance of the DASH system.
    OMB approval is requested for 3 years. There are no costs to 
respondents other than their time. The total estimated annualized 
burden hours are 211.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                   Frequency of    Average time
                  Type of form                       Number of     response per    per response    Total annual
                                                    respondents     respondent      (in hours)      burden hour
----------------------------------------------------------------------------------------------------------------
User Registration...............................             200               1            5/60              17
Data and Biospecimen Inventory Submissions......              36               1               2              72
Study Catalog Submission........................              10               1           30/60               5
Data Collection Catalog Submission..............               6               1           15/60               2
Data Request....................................              60               1               1              60

[[Page 3162]]

 
Biospecimen Request.............................              36               1               1              36
Data Use Annual Progress Report.................              60               1           10/60              10
Biospecimen Use Annual Progress Report..........              36               1           10/60               6
Institutional Certification Template............              36               1            5/60               3
                                                 ---------------------------------------------------------------
    Total.......................................             200             200  ..............             211
----------------------------------------------------------------------------------------------------------------


    Dated: January 5, 2021.
Jennifer M. Guimond,
Project Clearance Liaison, Eunice Kennedy Shriver National Institute of 
Child Health and Human Development, National Institutes of Health.
[FR Doc. 2021-00636 Filed 1-13-21; 8:45 am]
BILLING CODE 4140-01-P


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