Proposed Collection; 60-day Comment Request; Early Career Reviewer Program Online Application and Vetting System (Center for Scientific Review), 5677-5678 [2020-01798]

Download as PDF jbell on DSKJLSW7X2PROD with NOTICES Federal Register / Vol. 85, No. 21 / Friday, January 31, 2020 / Notices Registration to view the webcast: Deadline is February 21, 2020. Registration to view the meeting via the webcast is required. ADDRESSES: Meeting web page: The preliminary agenda, registration, and other meeting materials are available at https:// ntp.niehs.nih.gov/go/165. Webcast: The meeting will be webcast; the URL will be provided to those who register for viewing. FOR FURTHER INFORMATION CONTACT: Dr. Mary Wolfe, Designated Federal Official for the BSC, Office of Liaison, Policy and Review, Division of NTP, NIEHS, P.O. Box 12233, K2–03, Research Triangle Park, NC 27709. Phone: 984– 287–3209, Fax: 301–451–5759, Email: wolfe@niehs.nih.gov. Hand Deliver/ Courier address: 530 Davis Drive, Room K2130, Morrisville, NC 27560. SUPPLEMENTARY INFORMATION: The BSC will provide input to the NTP on programmatic activities and issues. The preliminary agenda topics include: Evolving the paradigm: In vivo to in vitro extrapolation, nano/microplastics and health effects: Novel agents bring novel challenges, traffic-related air pollution and hypertensive disorders of pregnancy: Disease as a toxicology focus, and NTP studies of per- and polyfluoroalkyl substances: Understanding human translation. The preliminary agenda, roster of BSC members, background materials, public comments, and any additional information, when available, will be posted on the BSC meeting website (https:// ntp.niehs.nih.gov/go/165) or may be requested in hardcopy from the Designated Federal Official for the BSC. Following the meeting, summary minutes will be prepared and made available on the BSC meeting website. Meeting Attendance Registration: The meeting is open to the public with time set aside for oral public comment. Registration to view the webcast is by February 21, 2020, at https:// ntp.niehs.nih.gov/go/165. Registration is required to view the webcast; the URL for the webcast will be provided in the email confirming registration. TTY users should contact the Federal TTY Relay Service at 800–877–8339. Requests should be made at least five business days in advance of the event. Written Public Comments: NTP invites written public comments. Guidelines for public comments are available at https://ntp.niehs.nih.gov/ ntp/about_ntp/guidelines_public_ comments_508.pdf. The deadline for submission of written comments is February 14, 2020. Written public comments should be VerDate Sep<11>2014 17:16 Jan 30, 2020 Jkt 250001 submitted through the meeting website. Persons submitting written comments should include name, affiliation, mailing address, phone, email, and sponsoring organization (if any). Written comments received in response to this notice will be posted on the NTP website, and the submitter will be identified by name, affiliation, and sponsoring organization (if any). Oral Public Comment Registration: The agenda allows for four formal public comment periods—one comment period per topic (up to 3 commenters, up to 5 minutes per speaker, per topic). Persons wishing to make an oral comment are required to register online at https://ntp.niehs.nih.gov/go/165 by February 14, 2020. Oral comments will be received only during the formal comment periods indicated on the preliminary agenda and presented via a teleconference line. The access number for the teleconference line will be provided to registrants by email prior to the meeting. Registration is on a firstcome, first-served basis. Each organization is allowed one time slot per topic. After the maximum number of speakers per comment period is exceeded, individuals registered to provide oral comment will be placed on a wait list and notified should an opening become available. Commenters will be notified approximately one week before the meeting about the actual time allotted per speaker. If possible, oral public commenters should send a copy of their slides and/ or statement or talking points to NTPMeetings@icf.com by February 14, 2020. Meeting Materials: The preliminary meeting agenda is available on the meeting web page (https:// ntp.niehs.nih.gov/go/165) and will be updated one week before the meeting. Individuals are encouraged to access the meeting web page to stay abreast of the most current information regarding the meeting. Background Information on the BSC: The BSC is a technical advisory body comprised of scientists from the public and private sectors that provides primary scientific oversight to the NTP. Specifically, the BSC advises the NTP on matters of scientific program content, both present and future, and conducts periodic review of the program for the purpose of determining and advising on the scientific merit of its activities and their overall scientific quality. Its members are selected from recognized authorities knowledgeable in fields such as toxicology, pharmacology, pathology, epidemiology, risk assessment, carcinogenesis, mutagenesis, cellular biology, computational toxicology, neurotoxicology, genetic toxicology, PO 00000 Frm 00067 Fmt 4703 Sfmt 4703 5677 reproductive toxicology or teratology, and biostatistics. Members serve overlapping terms of up to four years. The BSC usually meets biannually. The authority for the BSC is provided by 42 U.S.C. 217a, section 222 of the Public Health Service Act (PHS), as amended. The BSC is governed by the provisions of the Federal Advisory Committee Act, as amended (5 U.S.C. app.), which sets forth standards for the formation and use of advisory committees. Dated: January 21, 2020. Brian R. Berridge, Associate Director, National Toxicology Program. [FR Doc. 2020–01792 Filed 1–30–20; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Proposed Collection; 60-day Comment Request; Early Career Reviewer Program Online Application and Vetting System (Center for Scientific Review) AGENCY: National Institutes of Health, HHS. ACTION: 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 Center for Scientific Review (CSR) 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. SUMMARY: To obtain a copy of the data collection plans and instruments, submit comments in writing, or request more information on the proposed project, contact: Dr. Hope Cummings, Project Clearance Liaison, Center for Scientific Review, NIH, Room 4134, 6701 Rockledge Drive, Bethesda, Maryland, 20892 or call non-toll-free number (301) 402–4706 or Email your request, including your address to: hope.cummings@nih.gov. Formal requests for additional plans and instruments must be requested in writing. FOR FURTHER INFORMATION CONTACT: E:\FR\FM\31JAN1.SGM 31JAN1 5678 Federal Register / Vol. 85, No. 21 / Friday, January 31, 2020 / Notices 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 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 minimizes 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: Early Career Reviewer Program Online Application and Vetting System, 0925– 0695, REVISION, exp., date 05/31/2020, Center for Scientific Review (CSR), National Institutes of Health (NIH). SUPPLEMENTARY INFORMATION: Need and Use of Information Collection: The Center for Scientific Review (CSR) is the portal for NIH grant applications and their review for scientific merit. Our mission is to see that all NIH grant applications receive fair, independent, expert, and timely reviews—free from inappropriate influences—so NIH can fund the most promising research. To accomplish this goal, Scientific Review Officers (SRO) form study sections consisting of scientists who have the technical and scientific expertise to evaluate the merit of grant applications. Study section members are generally scientists who have established independent programs of research as demonstrated by their publications and their grant award experiences. The CSR Early Career Reviewer program was developed to identify and train qualified scientists who are early in their scientific careers and who have not had prior CSR review experience. The goals of the program are to expose these early career scientists to the peer review experience so that they become more competitive as applicants as well as to enrich the existing pool of NIH reviewers. Currently, the online application software, the Early Career Reviewer Application and Vetting System, is accessed online by applicants to the Early Career Reviewer Program who provide information such as their name, contact information, a description of their areas of expertise, their study section preferences, and their professional Curriculum Vitae. This Information Collection Request (ICR) is to revise the Early Career Reviewer Application and Vetting System to include additional questions and be more user friendly. Additional questions are in line with NIH’s renewed Interest in Diversity (NOT– OD–20–031) and include questions such as applicants’ race, ethnicity, gender, disability, and disadvantage backgrounds. Applicants can choose if they would like to answer these additional questions (i.e. optional). Applicants are also now able to check their eligibility before applying to the program. OMB approval is requested for 3 years. There are no costs to respondents other than their time. The total estimated annualized burden hours are 505. ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Type of respondent Average time per response (in hours) Total annual burden hour Research scientists .......................................................................................... 1212 1 25/60 505 Total .......................................................................................................... ........................ 1212 ........................ 505 Dated: January 22, 2020. Hope M. Cummings, Project Clearance Liaison, Center for Scientific Review (CSR), National Institutes of Health. [FR Doc. 2020–01798 Filed 1–30–20; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Substance Abuse and Mental Health Services Administration jbell on DSKJLSW7X2PROD with NOTICES Number of responses per respondent Current List of HHS-Certified Laboratories and Instrumented Initial Testing Facilities Which Meet Minimum Standards To Engage in Urine and Oral Fluid Drug Testing for Federal Agencies Substance Abuse and Mental Health Services Administration, HHS. AGENCY: ACTION: Notice. VerDate Sep<11>2014 17:16 Jan 30, 2020 Jkt 250001 The Department of Health and Human Services (HHS) notifies federal agencies of the laboratories and Instrumented Initial Testing Facilities (IITFs) currently certified to meet the standards of the Mandatory Guidelines for Federal Workplace Drug Testing Programs using Urine or Oral Fluid (Mandatory Guidelines). A notice listing all currently HHScertified laboratories and IITFs is published in the Federal Register during the first week of each month. If any laboratory or IITF certification is suspended or revoked, the laboratory or IITF will be omitted from subsequent lists until such time as it is restored to full certification under the Mandatory Guidelines. If any laboratory or IITF has withdrawn from the HHS National Laboratory Certification Program (NLCP) during the past month, it will be listed at the end and will be omitted from the monthly listing thereafter. SUMMARY: PO 00000 Frm 00068 Fmt 4703 Sfmt 4703 This notice is also available on the internet at https://www.samhsa.gov/ workplace/resources/drug-testing/ certified-lab-list. FOR FURTHER INFORMATION CONTACT: Anastasia Donovan, Division of Workplace Programs, SAMHSA/CSAP, 5600 Fishers Lane, Room 16N06B, Rockville, Maryland 20857; 240–276– 2600 (voice); Anastasia.Donovan@ samhsa.hhs.gov (email). SUPPLEMENTARY INFORMATION: The Department of Health and Human Services (HHS) notifies federal agencies of the laboratories and Instrumented Initial Testing Facilities (IITFs) currently certified to meet the standards of the Mandatory Guidelines for Federal Workplace Drug Testing Programs (Mandatory Guidelines) using Urine and of the laboratories currently certified to meet the standards of the Mandatory Guidelines using Oral Fluid. The Mandatory Guidelines using Urine were first published in the E:\FR\FM\31JAN1.SGM 31JAN1

Agencies

[Federal Register Volume 85, Number 21 (Friday, January 31, 2020)]
[Notices]
[Pages 5677-5678]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-01798]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Proposed Collection; 60-day Comment Request; Early Career 
Reviewer Program Online Application and Vetting System (Center for 
Scientific Review)

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 Center for Scientific Review (CSR) 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: Dr. Hope 
Cummings, Project Clearance Liaison, Center for Scientific Review, NIH, 
Room 4134, 6701 Rockledge Drive, Bethesda, Maryland, 20892 or call non-
toll-free number (301) 402-4706 or Email your request, including your 
address to: [email protected]. Formal requests for additional plans 
and instruments must be requested in writing.

[[Page 5678]]


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 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 minimizes 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: Early Career Reviewer Program Online 
Application and Vetting System, 0925-0695, REVISION, exp., date 05/31/
2020, Center for Scientific Review (CSR), National Institutes of Health 
(NIH).
    Need and Use of Information Collection: The Center for Scientific 
Review (CSR) is the portal for NIH grant applications and their review 
for scientific merit. Our mission is to see that all NIH grant 
applications receive fair, independent, expert, and timely reviews--
free from inappropriate influences--so NIH can fund the most promising 
research. To accomplish this goal, Scientific Review Officers (SRO) 
form study sections consisting of scientists who have the technical and 
scientific expertise to evaluate the merit of grant applications. Study 
section members are generally scientists who have established 
independent programs of research as demonstrated by their publications 
and their grant award experiences.
    The CSR Early Career Reviewer program was developed to identify and 
train qualified scientists who are early in their scientific careers 
and who have not had prior CSR review experience. The goals of the 
program are to expose these early career scientists to the peer review 
experience so that they become more competitive as applicants as well 
as to enrich the existing pool of NIH reviewers. Currently, the online 
application software, the Early Career Reviewer Application and Vetting 
System, is accessed online by applicants to the Early Career Reviewer 
Program who provide information such as their name, contact 
information, a description of their areas of expertise, their study 
section preferences, and their professional Curriculum Vitae. This 
Information Collection Request (ICR) is to revise the Early Career 
Reviewer Application and Vetting System to include additional questions 
and be more user friendly. Additional questions are in line with NIH's 
renewed Interest in Diversity (NOT-OD-20-031) and include questions 
such as applicants' race, ethnicity, gender, disability, and 
disadvantage backgrounds. Applicants can choose if they would like to 
answer these additional questions (i.e. optional). Applicants are also 
now able to check their eligibility before applying to the program.
    OMB approval is requested for 3 years. There are no costs to 
respondents other than their time. The total estimated annualized 
burden hours are 505.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                     Number of     Average time
               Type of respondent                    Number of     responses per   per response    Total annual
                                                    respondents     respondent      (in hours)      burden hour
----------------------------------------------------------------------------------------------------------------
Research scientists.............................            1212               1           25/60             505
                                                 ---------------------------------------------------------------
    Total.......................................  ..............            1212  ..............             505
----------------------------------------------------------------------------------------------------------------


    Dated: January 22, 2020.
Hope M. Cummings,
Project Clearance Liaison, Center for Scientific Review (CSR), National 
Institutes of Health.
[FR Doc. 2020-01798 Filed 1-30-20; 8:45 am]
BILLING CODE 4140-01-P


This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.