Submission for OMB Review; 30-Day Comment Request: Generic Clearance for Satisfaction Surveys of Customers (CSR), 64202-64203 [2014-25601]

Download as PDF 64202 Federal Register / Vol. 79, No. 208 / Tuesday, October 28, 2014 / Notices withdrawn from sale for reasons of safety or effectiveness. Accordingly, the Agency will continue to list DIAMOX (acetazolamide) intravenous, 500 mg base/vial, and DIAMOX (acetazolamide) tablets, 125 mg and 250 mg, in the ‘‘Discontinued Drug Product List’’ section of the Orange Book. The ‘‘Discontinued Drug Product List’’ delineates, among other items, drug products that have been discontinued from marketing for reasons other than safety or effectiveness. FDA will not begin procedures to withdraw approval of ANDAs that refer to DIAMOX (acetazolamide) intravenous, 500 mg base/vial, and DIAMOX (acetazolamide) tablets, 125 mg and 250 mg. Additional ANDAs that refer to these products may also be approved by the Agency as long as they meet all other legal and regulatory requirements for the approval of ANDAs. If FDA determines that labeling for these drug products should be revised to meet current standards, the Agency will advise ANDA applicants to submit such labeling. Dated: October 21, 2014. Leslie Kux, Assistant Commissioner for Policy. [FR Doc. 2014–25534 Filed 10–27–14; 8:45 am] BILLING CODE 4164–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Submission for OMB Review; 30-Day Comment Request: Generic Clearance for Satisfaction Surveys of Customers (CSR) Under the provisions of Section 3507(a)(l)(D) of the Paperwork Reduction Act of 1995, the National Institutes of Health (NIH) has submitted to the Office of Management and Budget (OMB) a request for review and SUMMARY: approval of the information collection listed below. This proposed information collection was previously published in the Federal Register on August 21, 2014, page 49523 and allowed 60 days for public comment. No public comments were received. The purpose of this notice is to allow an additional 30 days for public comment. The Center for Scientific Review (CSR), National Institutes of Health, may not conduct or sponsor, and the respondent is not required to respond to, an information collection that has been extended, revised, or implemented on or after October 31, 2014, unless it displays a currently valid OMB control number. 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: NIH Desk Officer. DATES: Comment 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. 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. Mary Ann Guadagno, Project Clearance Liaison, Center for Scientific Review, NIH, Room 3182, 6701 Rockledge Drive, Bethesda, MD 20892, or call non-toll-free number (301) 435–1251 or Email your request, including your address to: guadagma@ csr.nih.gov. Formal requests for additional plans and instruments must be requested in writing. Proposed Collection: Generic Clearance for Satisfaction Surveys of Customers (CSR), 0925–0474— extension, Center for Scientific Review (CSR), National Institutes of Health (NIH). Need and Use of Information Collection: The information collected in these surveys will be used by the Center for Scientific Review management and personnel: (1) To assess the quality of the modified operations and processes now used by CSR to review grant applications; (2) To assess the quality of service provided by CSR to our customers; (3) To enable identification of the most promising biomedical research that will have the greatest impact on improving public health by using a peer review process that is fair unbiased from outside influence, timely, and (4) To develop new modes of operation based on customer need and customer feedback about the efficacy of implemented modifications. These surveys will almost certainly lead to quality improvement activities to enhance and/or streamline CSR’s operations. The major mechanism by which CSR will request input is through surveys. The major initiatives ongoing at the present time include: Evaluation of the peer review process, surveys of new and early stage investigators, satisfaction with study section meetings using alternative review platforms, quick feedback for peer review, satisfaction with new reviewer orientation sessions, teleworker space needs, improving study section alignment to ensure the best reviews, and others. Surveys will be collected via Internet or in focus groups. Information gathered from these surveys will be presented to, and used directly by, CSR management to enhance the operations, processes, organization of, and services provided by the Center. OMB approval is requested for 3 years. There are no costs to respondents other than their time. The total estimated annualized burden hours are 4323. ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Type of respondent A ............... B ............... asabaliauskas on DSK4SPTVN1PROD with NOTICES Form name Adult scientific professionals (via Mail/Telephone/Internet) ...... Adult scientific professionals (via focus groups) ....................... VerDate Sep<11>2014 20:06 Oct 27, 2014 Jkt 235001 PO 00000 Frm 00040 Fmt 4703 Sfmt 4703 Number of responses per respondent 7925 240 E:\FR\FM\28OCN1.SGM Average burden per response (in hours) 1 1 28OCN1 30/60 90/60 Total annual burden hour 3963 360 Federal Register / Vol. 79, No. 208 / Tuesday, October 28, 2014 / Notices 64203 Dated: October 20, 2014. Mary Ann Guadagno, Project Clearance Liaison, Center for Scientific Review, National Institutes of Health. Dated: October 22, 2014. Melanie J. Gray, Program Analyst, Office of Federal Advisory Committee Policy. DEPARTMENT OF HEALTH AND HUMAN SERVICES [FR Doc. 2014–25505 Filed 10–27–14; 8:45 am] [FR Doc. 2014–25601 Filed 10–27–14; 8:45 am] BILLING CODE 4140–01–P National Institute of Allergy and Infectious Diseases; Notice of Closed Meeting BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institutes of Health National Institute of Allergy and Infectious Diseases; Notice of Closed Meeting National Cancer Institute; Notice of Meeting asabaliauskas on DSK4SPTVN1PROD with NOTICES Pursuant to section 10(a) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), notice is hereby given of a meeting of the President’s Cancer Panel. The meeting will be open to the public, with attendance limited to space available. Individuals who plan to attend and need special assistance, such as sign language interpretation or other reasonable accommodations, should notify the Contact Person listed below in advance of the meeting. Name of Committee: President’s Cancer Panel. Date: December 11, 2014. Time: 8:30 a.m. to 4:00 p.m. Agenda: Connected Health: Improving Patients’ Engagement and Activation for Cancer-Related Health. Place: Royal Sonesta Hotel Boston, 40 Edwin Land Blvd., Cambridge, MA 02142. Contact Person: Abby B. Sandler, Ph.D., Executive Secretary, President’s Cancer Panel, Special Assistant to the Director, NCI Center for Cancer Research, 9000 Rockville Pike, Building 31, Room B2B37, MSC 2590, Bethesda, MD 20892–8349, (301) 451–9399, sandlera@mail.nih.gov. Any interested person may file written comments with the committee by forwarding the statement to the Contact Person listed on this notice. The statement should include the name, address, telephone number and when applicable, the business or professional affiliation of the interested person. Information is also available on the Institute’s/Center’s home page: https:// deainfo.nci.nih.gov/advisory/pcp/index.htm, where an agenda and any additional information for the meeting will be posted when available. (Catalogue of Federal Domestic Assistance Program Nos. 93.392, Cancer Construction; 93.393, Cancer Cause and Prevention Research; 93.394, Cancer Detection and Diagnosis Research; 93.395, Cancer Treatment Research; 93.396, Cancer Biology Research; 93.397, Cancer Centers Support; 93.398, Cancer Research Manpower; 93.399, Cancer Control, National Institutes of Health, HHS) VerDate Sep<11>2014 20:06 Oct 27, 2014 Jkt 235001 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 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; NIAID Peer Review Meeting. Date: November 18–19, 2014. Time: 8:00 a.m. to 5:00 p.m. Agenda: To review and evaluate contract proposals. Place: Doubletree by Hilton Bethesda— Washington, DC, 8120 Wisconsin Avenue, Bethesda, MD 20814, 301–664–7310, Fax: 301–664–7317. Contact Person: Susana Mendez, Ph.D., Scientific Review Officer, Scientific Review Program, Division of Extramural Activities, DHHS/NIH/NIAID, 5601 Fishers Lane, MSC 9823, Rockville, MD 20852, 240–669–5077, Fax: 301–480–2408, susana.mendez@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: October 22, 2014. David Clary, Program Analyst, Office of Federal Advisory Committee Policy. [FR Doc. 2014–25509 Filed 10–27–14; 8:45 am] National Institutes of Health 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: National Institute of Allergy and Infectious Diseases Special Emphasis Panel, NIAID Division of Allergy, Immunology and Transplantation: Statistical and Clinical Coordinating Center. Date: November 17, 2014. Time: 11:00 a.m. to 5:00 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, 5601 Fisher Lane, MSC 9823, Room 3F100, Rockville, MD 20852, (Telephone Conference Call). Contact Person: Paul A. Amstad, Ph.D., Scientific Review Officer, Scientific Review Program, Division of Extramural Activities, National Institutes of Health/NIAID, 5601 Fisher Lane, MSC 9823, Rockville, MD 20852, 240–669–5067, PAmstad@ 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: October 22, 2014. David Clary, Program Analyst, Office of Federal Advisory Committee Policy. [FR Doc. 2014–25507 Filed 10–27–14; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute of General Medical Sciences; Notice of Closed Meeting BILLING CODE 4140–01–P PO 00000 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. Frm 00041 Fmt 4703 Sfmt 4703 E:\FR\FM\28OCN1.SGM 28OCN1

Agencies

[Federal Register Volume 79, Number 208 (Tuesday, October 28, 2014)]
[Notices]
[Pages 64202-64203]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-25601]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Submission for OMB Review; 30-Day Comment Request: Generic 
Clearance for Satisfaction Surveys of Customers (CSR)

SUMMARY: Under the provisions of Section 3507(a)(l)(D) of the Paperwork 
Reduction Act of 1995, the National Institutes of Health (NIH) has 
submitted to the Office of Management and Budget (OMB) a request for 
review and approval of the information collection listed below. This 
proposed information collection was previously published in the Federal 
Register on August 21, 2014, page 49523 and allowed 60 days for public 
comment. No public comments were received. The purpose of this notice 
is to allow an additional 30 days for public comment. The Center for 
Scientific Review (CSR), National Institutes of Health, may not conduct 
or sponsor, and the respondent is not required to respond to, an 
information collection that has been extended, revised, or implemented 
on or after October 31, 2014, unless it displays a currently valid OMB 
control number.
    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: NIH Desk Officer.

DATES: Comment 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.

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. Mary Ann 
Guadagno, Project Clearance Liaison, Center for Scientific Review, NIH, 
Room 3182, 6701 Rockledge Drive, Bethesda, MD 20892, or call non-toll-
free number (301) 435-1251 or Email your request, including your 
address to: guadagma@csr.nih.gov. Formal requests for additional plans 
and instruments must be requested in writing.
    Proposed Collection: Generic Clearance for Satisfaction Surveys of 
Customers (CSR), 0925-0474--extension, Center for Scientific Review 
(CSR), National Institutes of Health (NIH).
    Need and Use of Information Collection: The information collected 
in these surveys will be used by the Center for Scientific Review 
management and personnel: (1) To assess the quality of the modified 
operations and processes now used by CSR to review grant applications; 
(2) To assess the quality of service provided by CSR to our customers; 
(3) To enable identification of the most promising biomedical research 
that will have the greatest impact on improving public health by using 
a peer review process that is fair unbiased from outside influence, 
timely, and (4) To develop new modes of operation based on customer 
need and customer feedback about the efficacy of implemented 
modifications. These surveys will almost certainly lead to quality 
improvement activities to enhance and/or streamline CSR's operations. 
The major mechanism by which CSR will request input is through surveys. 
The major initiatives ongoing at the present time include: Evaluation 
of the peer review process, surveys of new and early stage 
investigators, satisfaction with study section meetings using 
alternative review platforms, quick feedback for peer review, 
satisfaction with new reviewer orientation sessions, teleworker space 
needs, improving study section alignment to ensure the best reviews, 
and others. Surveys will be collected via Internet or in focus groups. 
Information gathered from these surveys will be presented to, and used 
directly by, CSR management to enhance the operations, processes, 
organization of, and services provided by the Center.
    OMB approval is requested for 3 years. There are no costs to 
respondents other than their time. The total estimated annualized 
burden hours are 4323.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                      Average
                                                     Number of       Number of      burden per     Total annual
      Form name           Type of respondent        respondents   responses  per   response (in     burden hour
                                                                     respondent       hours)
----------------------------------------------------------------------------------------------------------------
A...................  Adult scientific                      7925               1           30/60            3963
                       professionals (via Mail/
                       Telephone/Internet).
B...................  Adult scientific                       240               1           90/60             360
                       professionals (via focus
                       groups).
----------------------------------------------------------------------------------------------------------------



[[Page 64203]]

    Dated: October 20, 2014.
Mary Ann Guadagno,
Project Clearance Liaison, Center for Scientific Review, National 
Institutes of Health.
[FR Doc. 2014-25601 Filed 10-27-14; 8:45 am]
BILLING CODE 4140-01-P
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