Submission for OMB review; Comment Request; Process Evaluation of the NIH Roadmap Epigenomics Program, 30178-30179 [2011-12722]

Download as PDF 30178 Federal Register / Vol. 76, No. 100 / Tuesday, May 24, 2011 / Notices To request more information on the proposed project or to obtain a copy of the data collection plans and instruments, contact Quandra Scudder, Project Officer, National Institute on Drug Abuse NIDA, NIH, 6001 Executive Boulevard, Bethesda, MD 20892–9557, or call non-toll-free number (301) 594– 0394 or E-mail your request, including your address to scudderq@nida.nih.gov. Comments Due Date: 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: Dated: May 18, 2011. Mary Affeldt, Executive Officer, (OM Director) NIDA. [FR Doc. 2011–12726 Filed 5–23–11; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Submission for OMB review; Comment Request; Process Evaluation of the NIH Roadmap Epigenomics Program Under the provisions of Section 3507(a)(1)(D) of the Paperwork Reduction Act of 1995, the National Institute on Drug Abuse (NIDA), the National Institutes of Health (NIH), has submitted to the Office of Management and Budget (OMB) a request to review and approve the information collection listed below. This proposed information collection was previously published in the Federal Register in Vol. 76, No. 49, pages 13648–13649 on March 14, 2011, and allowed 60 days for public SUMMARY: comment. No public comments were received on the planned study or any of the specific topics outlined in the 60day notice. The purpose of this notice is to allow an additional 30 days for public comment. 5 CFR 1320.5 (General requirements) Reporting and Recordkeeping Requirements: Final Rule requires that the agency inform the potential persons who are to respond to the collection of information that such persons are not required to respond to the collection of information unless it displays a currently valid OMB control number. Proposed Collection Title: Process Evaluation of the NIH Roadmap Epigenomics Program. Type of Information Collection Request: New. Need and Use of Information Collection: The proposed information collection is essential to the process evaluation of the NIH Roadmap Epigenomics Program. The process evaluation is a requirement of each of the relevant RFAs funded under the NIH Roadmap Epigenomics Program which require participating in evaluation research activities. This evaluation study, a mixedmethods study which uses secondary source documentation and information from tracking and monitoring systems along with primary data to assess program process and progress, is nonexperimental. The assessment is based on secondary source information, with primary source information collection added to augment the reliability and internal validity. The primary data collection uses information categories that genuinely tap added distinctions and opinions that relate to it to build the weight of evidence from first-hand sources that substantiate the initial hypotheses about the program phenomenon and its differences from a typical research portfolio of individual and insular projects. The synthesized results across primary and secondary data sources will provide critical insights on transformativeness of high-impact, trans-NIH programs and contribute important information about the synergies and collaborations in multicomponent scientific research. It will also identify areas for program improvement and lessons learned that might be useful to other research programs of the Agency. To reduce response bias and to make the survey as accessible as possible to busy principal investigators, the survey will be web-based. Frequency of Response: Once. Affected Public: Principal Investigators of the program at not-forprofit institutions. Type of Respondents: Principle Investigators. The annual reporting burden is as follows: Estimated Number of Respondents: 53. Estimated Number of Responses per Respondent: 1. Average Burden Hours per Response: .33. Estimated Total Annual Burden Hours Requested: 17.49. The annualized cost to respondents is estimated at: $891.99. There are no Capital Costs, Operating Costs and/or Maintenance Costs to report. ESTIMATED ANNUALIZED BURDEN HOURS AND COSTS Type of respondent Number of respondents Number of responses per respondent 53 1 Principal Investigators .. jlentini on DSK4TPTVN1PROD with NOTICES 1 20 Total number of responses Avg. burden hours per response 1 Annual burden hours requested 133 17.49 Avg. hourly wage rate 51 Total annual respondent cost 891.99 minutes. Request for Comments: Written comments and/or suggestions from the public and affected agencies are invited on 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 VerDate Mar<15>2010 16:47 May 23, 2011 Jkt 223001 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. Direct Comments to OMB: Written comments and/or suggestions regarding the item(s) contained in this notice, PO 00000 Frm 00091 Fmt 4703 Sfmt 4703 especially regarding the estimated public burden and associated response time, should be directed to the: Office of Management and Budget, Office of Regulatory Affairs, OIRA_submission@ omb.eop.gov or by fax to 202–395–6974, Attention: Desk Officer for NIH. To request more information on the proposed project or to obtain a copy of the data collection plans and instruments, contact Genevieve deAlmeida-Morris, PhD, M.P.H., Project Officer, Office of Science Policy and E:\FR\FM\24MYN1.SGM 24MYN1 Federal Register / Vol. 76, No. 100 / Tuesday, May 24, 2011 / Notices Communications, NIH/NIDA, NSC— Neuroscience Center, 5229, 6001 Executive Blvd., Rockville, MD, 20852, or call non-toll-free number 301–594– 6802 or e-mail your request including your address to: dealmeig@nida.nih.gov. Comments Due Date: Comments regarding this information collection are best assured of having their full effect if received within 30 days of the date of this publication. Dated: May 18, 2011. Mary Affeldt, Executive Officer, (OM Director, NIDA). BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute on Deafness and Other Communication Disorders Notice of Closed Meeting jlentini on DSK4TPTVN1PROD with NOTICES Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), 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: Communication Disorders Review Committee. Date: June 15–16, 2011. Time: June 15, 2011, 8 a.m. to 5 p.m. Agenda: To review and evaluate grant applications. Place: Hyatt Regency Bethesda, One Bethesda Metro Center, 7400 Wisconsin Avenue, Bethesda, MD 20814. Time: June 16, 2011, 8 a.m. to 5 p.m. Agenda: To review and evaluate grant applications. Place: Hyatt Regency Bethesda, One Bethesda Metro Center, 7400 Wisconsin Avenue, Bethesda, MD 20814. Contact Person: Susan Sullivan, PhD, Scientific Review Branch Division of Extramural Activities, NIDCD, NIH, 6120 Executive Blvd., Suite 400C, Bethesda, MD 20892, 301–496–8683, sullivas@mail.nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.173, Biological Research Related to Deafness and Communicative Disorders, National Institutes of Health, HHS) 16:47 May 23, 2011 Jkt 223001 [FR Doc. 2011–12740 Filed 5–23–11; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute on Deafness and Other Communication Disorders; Notice of Closed Meetings [FR Doc. 2011–12722 Filed 5–23–11; 8:45 am] VerDate Mar<15>2010 Dated: May 18, 2011. Jennifer S. Spaeth, Director, Office of Federal Advisory Committee Policy. Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), 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 on Deafness and Other Communication Disorders Special Emphasis Panel, R03–VSL. Date: June 1, 2011. Time: 11 a.m. to 4 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, 6120 Executive Blvd., Rockville, MD 20852, (Telephone Conference Call). Contact Person: Shiguang Yang, DVM, PhD, Scientific Review Officer, Division of Extramural Activities, NIDCD, NIH, 6120 Executive Blvd., Bethesda, MD 20892, 301– 496–8683. This notice is being published less than 15 days prior to the meeting due to the timing limitations imposed by the review and funding cycle. Name of Committee: National Institute on Deafness and Other Communication Disorders Special Emphasis Panel, R03Chemical Senses. Date: June 2, 2011. Time: 12 p.m. to 2 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, 6120 Executive Blvd., Rockville, MD 20852, (Telephone Conference Call). Contact Person: Susan L. Sullivan, PhD, Scientific Review Officer, National Institute of Deafness and Other, Communication Disorders, 6120 Executive Blvd Ste., 400C, Rockville, MD 20852, 301–496–8683, sullivas@mail.nih.gov. This notice is being published less than 15 days prior to the meeting due to the timing PO 00000 Frm 00092 Fmt 4703 Sfmt 9990 30179 limitations imposed by the review and funding cycle. Name of Committee: National Institute on Deafness and Other Communication Disorders Special Emphasis Panel, R03– Hearing and Balance. Date: June 3, 2011. Time: 11 a.m. to 2 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, 6120 Executive Blvd., Rockville, MD 20852, (Telephone Conference Call). Contact Person: Sheo Singh, PhD, Scientific Review Officer, Scientific Review Branch, Division of Extramural Activities, Executive Plaza South, Room 400C, 6120 Executive Blvd., Bethesda, MD 20892, 301– 496–8683, singhs@nidcd.nih.gov. This notice is being published less than 15 days prior to the meeting due to the timing limitations imposed by the review and funding cycle. (Catalogue of Federal Domestic Assistance Program Nos. 93.173, Biological Research Related to Deafness and Communicative Disorders, National Institutes of Health, HHS) Dated: May 18, 2011. Jennifer S. Spaeth, Director, Office of Federal Advisory Committee Policy. [FR Doc. 2011–12739 Filed 5–23–11; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Center for Scientific Review; Amended Notice of Meeting Notice is hereby given of a change in the meeting of the Xenobiotic and Nutrient Disposition and Action Study Section, June 8, 2011, 8 a.m. to June 8, 2011, 6 p.m., Sir Francis Drake Hotel, 450 Powell Street, San Francisco, CA, 94102 which was published in the Federal Register on April 29, 2011, 76 FR 24036–24038. The meeting will be held at The Westin St. Francis Hotel, 335 Powell Street, San Francisco, CA 94102. The meeting date and time remain the same. The meeting is closed to the public. Dated: May 17, 2011. Jennifer S. Spaeth, Director, Office of Federal Advisory Committee Policy. [FR Doc. 2011–12737 Filed 5–23–11; 8:45 am] BILLING CODE 4140–01–P E:\FR\FM\24MYN1.SGM 24MYN1

Agencies

[Federal Register Volume 76, Number 100 (Tuesday, May 24, 2011)]
[Notices]
[Pages 30178-30179]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-12722]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Submission for OMB review; Comment Request; Process Evaluation of 
the NIH Roadmap Epigenomics Program

SUMMARY: Under the provisions of Section 3507(a)(1)(D) of the Paperwork 
Reduction Act of 1995, the National Institute on Drug Abuse (NIDA), the 
National Institutes of Health (NIH), has submitted to the Office of 
Management and Budget (OMB) a request to review and approve the 
information collection listed below. This proposed information 
collection was previously published in the Federal Register in Vol. 76, 
No. 49, pages 13648-13649 on March 14, 2011, and allowed 60 days for 
public comment. No public comments were received on the planned study 
or any of the specific topics outlined in the 60-day notice. The 
purpose of this notice is to allow an additional 30 days for public 
comment. 5 CFR 1320.5 (General requirements) Reporting and 
Recordkeeping Requirements: Final Rule requires that the agency inform 
the potential persons who are to respond to the collection of 
information that such persons are not required to respond to the 
collection of information unless it displays a currently valid OMB 
control number.

Proposed Collection

    Title: Process Evaluation of the NIH Roadmap Epigenomics Program.
    Type of Information Collection Request: New.
    Need and Use of Information Collection: The proposed information 
collection is essential to the process evaluation of the NIH Roadmap 
Epigenomics Program. The process evaluation is a requirement of each of 
the relevant RFAs funded under the NIH Roadmap Epigenomics Program 
which require participating in evaluation research activities.
    This evaluation study, a mixed-methods study which uses secondary 
source documentation and information from tracking and monitoring 
systems along with primary data to assess program process and progress, 
is non-experimental. The assessment is based on secondary source 
information, with primary source information collection added to 
augment the reliability and internal validity. The primary data 
collection uses information categories that genuinely tap added 
distinctions and opinions that relate to it to build the weight of 
evidence from first-hand sources that substantiate the initial 
hypotheses about the program phenomenon and its differences from a 
typical research portfolio of individual and insular projects.
    The synthesized results across primary and secondary data sources 
will provide critical insights on transformativeness of high-impact, 
trans-NIH programs and contribute important information about the 
synergies and collaborations in multi-component scientific research. It 
will also identify areas for program improvement and lessons learned 
that might be useful to other research programs of the Agency.
    To reduce response bias and to make the survey as accessible as 
possible to busy principal investigators, the survey will be web-based.
    Frequency of Response: Once.
    Affected Public: Principal Investigators of the program at not-for-
profit institutions.
    Type of Respondents: Principle Investigators.
    The annual reporting burden is as follows:
    Estimated Number of Respondents: 53.
    Estimated Number of Responses per Respondent: 1.
    Average Burden Hours per Response: .33.
    Estimated Total Annual Burden Hours Requested: 17.49.
    The annualized cost to respondents is estimated at: $891.99.
    There are no Capital Costs, Operating Costs and/or Maintenance 
Costs to report.

                                                       Estimated Annualized Burden Hours and Costs
--------------------------------------------------------------------------------------------------------------------------------------------------------
                                                             Number of                      Avg. burden    Annual burden                   Total annual
           Type of respondent                Number of     responses per   Total number      hours per         hours        Avg. hourly     respondent
                                            respondents     respondent     of responses      response        requested       wage rate         cost
--------------------------------------------------------------------------------------------------------------------------------------------------------
Principal Investigators.................              53               1               1             133           17.49              51          891.99
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ 20 minutes.

    Request for Comments: Written comments and/or suggestions from the 
public and affected agencies are invited on 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 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.
    Direct Comments to OMB: Written comments and/or suggestions 
regarding the item(s) contained in this notice, especially regarding 
the estimated public burden and associated response time, should be 
directed to the: Office of Management and Budget, Office of Regulatory 
Affairs, OIRA_submission@omb.eop.gov or by fax to 202-395-6974, 
Attention: Desk Officer for NIH. To request more information on the 
proposed project or to obtain a copy of the data collection plans and 
instruments, contact Genevieve deAlmeida-Morris, PhD, M.P.H., Project 
Officer, Office of Science Policy and

[[Page 30179]]

Communications, NIH/NIDA, NSC--Neuroscience Center, 5229, 6001 
Executive Blvd., Rockville, MD, 20852, or call non-toll-free number 
301-594-6802 or e-mail your request including your address to: 
dealmeig@nida.nih.gov.
    Comments Due Date: Comments regarding this information collection 
are best assured of having their full effect if received within 30 days 
of the date of this publication.

    Dated: May 18, 2011.
Mary Affeldt,
Executive Officer, (OM Director, NIDA).
[FR Doc. 2011-12722 Filed 5-23-11; 8:45 am]
BILLING CODE 4140-01-P
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