Proposed Collection; 60-Day Comment Request: Clearance for Surveys of Customers and Partners of the Office of Extramural Research of the National Institutes of Health, 70062-70063 [2013-27965]

Download as PDF 70062 Federal Register / Vol. 78, No. 226 / Friday, November 22, 2013 / Notices Families is soliciting public comment on the specific aspects of the information collection described above. Copies of the proposed collection of information can be obtained and comments may be forwarded by writing to the Administration for Children and Families, Office of Planning, Research and Evaluation, 370 L’Enfant Promenade SW., Washington, DC 20447, Attn: ACF Reports Clearance Officer. Email address: infocollection@ acf.hhs.gov. All requests should be identified by the title of the information collection. The Department specifically requests comments on: (a) Whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; (b) the accuracy of the agency’s estimate of the burden of the proposed collection of information; (c) the quality, utility, and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology. Consideration will be given to comments and suggestions submitted within 60 days of this publication. Rockville, MD 20855, 240–276–9079, john.bartkowiak@fda.hhs.gov. SUPPLEMENTARY INFORMATION: Zoetis Inc., 333 Portage St., Kalamazoo, MI 49007, has requested that FDA withdraw approval of the following three NADAs because the products, used to manufacture Type B and Type C medicated feeds, are no longer manufactured or marketed: NADA 007– 891 for 3–NITRO (roxarsone) Type A medicated article, NADA 092–953 for Roxarsone Type A Medicated Articles, and NADA 010–285 for CARB–O–SEP (carbarsone) Type A medicated article. Therefore, under authority delegated to the Commissioner of Food and Drugs and redelegated to the Center for Veterinary Medicine, and in accordance with § 514.116 Notice of withdrawal of approval of application (21 CFR 514.116), notice is given that approval of NADAs 007–891, 092–953, and 010– 285, and all supplements and amendments thereto, is hereby withdrawn. Elsewhere in this issue of the Federal Register, FDA is amending the animal drug regulations to reflect the voluntary withdrawal of approval of these applications. Robert Sargis, Reports Clearance Officer. [FR Doc. 2013–27916 Filed 11–21–13; 8:45 am] Dated: November 18, 2013. Bernadette Dunham, Director, Center for Veterinary Medicine. BILLING CODE 4160–01–P [FR Doc. 2013–28062 Filed 11–21–13; 8:45 am] BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Food and Drug Administration [Docket No. FDA–2013–N–0002] Withdrawal of Approval of New Animal Drug Applications; Carbarsone; Roxarsone AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA) is withdrawing approval of three new animal drug applications (NADAs) for roxarsone or carbarsone Type A medicated articles at the sponsor’s request because the products are no longer manufactured or marketed. DATES: Withdrawal of approval is effective December 2, 2013. FOR FURTHER INFORMATION CONTACT: John Bartkowiak, Center for Veterinary Medicine (HFV–212), Food and Drug Administration, 7519 Standish Pl., emcdonald on DSK67QTVN1PROD with NOTICES SUMMARY: VerDate Mar<15>2010 16:47 Nov 21, 2013 Jkt 232001 Proposed Collection; 60-Day Comment Request: Clearance for Surveys of Customers and Partners of the Office of Extramural Research of the National Institutes of Health In compliance with the requirement of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, for opportunity for public comment on proposed data collection projects, the Office of Extramural Research (OER), the National Institutes of Health (NIH) will publish periodic summaries of proposed projects to be submitted to the Office of Management and Budget (OMB) for review and approval. 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 SUMMARY: PO 00000 Frm 00051 Fmt 4703 Sfmt 4703 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. To submit comments in writing, request more information on the proposed project, or to obtain a copy of the data collection plans and instruments, contact Dr. Sherry Mills, Director, Office of Extramural Programs, OER, NIH, 6705 Rockledge Drive, Suite 350, Bethesda, MD 20892, or call nontoll-free number (301) 435–2729, or Email your request, including your address to: OEPMailbox@mail.nih.gov. Comments regarding this information collection are best assured of having their full effect if received within 60days of the date of this publication. Proposed Collection: Generic Clearance for Surveys of Customers and Partners of the Office of Extramural Research of the National Institutes of Health—Extension—0925–0627—Office of the Director (OD), Office of Extramural Research (OER), Office of Extramural Programs (OEP), National Institutes of Health (NIH). Need and Use of Information Collection: OER develops, coordinates the implementation of, and evaluates NIH-wide policies and procedures for the award of extramural funds. To move forward with our initiatives to ensure success in accomplishing the NIH mission, input from partners and customers is essential. Quality management principles have been integrated into OER’s culture and these surveys will provide customer satisfaction input on various elements of OER’s business processes. The approximately 14 (10 quantitative and 4 qualitative) customer satisfaction surveys that will be conducted under this generic clearance will gather and measure customer and partner satisfaction with OER processes and operations. The data collected from these surveys will provide the feedback to track and gauge satisfaction with NIH’s statutorily mandated operations and processes. OER/OD/NIH will present data and outcomes from these surveys to inform the NIH staff, officers, leadership, advisory committees, and other decision-making bodies as appropriate. Based on feedback from these stakeholders, OER/OD/NIH will E:\FR\FM\22NON1.SGM 22NON1 70063 Federal Register / Vol. 78, No. 226 / Friday, November 22, 2013 / Notices formulate improvement plans and take action when necessary. OMB approval is requested for 3 years. There are no costs to respondents other than their time. The total estimated annualized burden hours are 2,485. Estimated Annualized Burden Hours QUANTITATIVE SURVEY Number of respondents Type of respondent Science professionals, applicants, reviewers, Institutional Officials ................ Adult Science Trainees .................................................................................... General Public ................................................................................................. Number of responses per respondent 3,820 2,000 4,000 1 1 1 Average burden per response (in hours) Total annual burden hour 15/60 15/60 15/60 955 500 1,000 QUALITATIVE SURVEY Number of respondents Type of respondent Science professionals, applicants, reviewers, Institutional Officials ................ Adult Science Trainees .................................................................................... General Public ................................................................................................. Dated: November 13, 2013. Seleda Perryman, Chief, Project Clearance Officer, Office of Policy for Extramural Research Administration, National Institutes of Health. [FR Doc. 2013–27965 Filed 11–21–13; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health emcdonald on DSK67QTVN1PROD with NOTICES National Institute of Diabetes and Digestive and Kidney Diseases; Notice of Closed Meetings 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 of Diabetes and Digestive and Kidney Diseases Special Emphasis Panel; NIDDK Career Awards Review. Date: December 4, 2013. Time: 4:00 p.m. to 6:00 p.m. Agenda: To review and evaluate grant applications. VerDate Mar<15>2010 16:47 Nov 21, 2013 Jkt 232001 12 6 12 Place: National Institutes of Health, Two Democracy Plaza, 6707 Democracy Boulevard, Bethesda, MD 20892, (Telephone Conference Call). Contact Person: Carol J. Goter-Robinson, Ph.D., Scientific Review Officer, Review Branch, DEA, NIDDK, National Institutes of Health, Room 748, 6707 Democracy Boulevard, Bethesda, MD 20892–5452, (301) 594–7791, goterrobinsonc@ extra.niddk.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. Name of Committee: National Institute of Diabetes and Digestive and Kidney Diseases Special Emphasis Panel; Time-Sensitive Obesity. Date: December 11, 2013. Time: 3:30 p.m. to 5:00 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, Two Democracy Plaza, 6707 Democracy Boulevard, Bethesda, MD 20892, (Telephone Conference Call). Contact Person: Michele L. Barnard, Ph.D., Scientific Review Officer, Review Branch, DEA, NIDDK, National Institutes of Health, Room 753, 6707 Democracy Boulevard, Bethesda, MD 20892–2542, (301) 594–8898, barnardm@extra.niddk.nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.847, Diabetes, Endocrinology and Metabolic Research; 93.848, Digestive Diseases and Nutrition Research; 93.849, Kidney Diseases, Urology and Hematology Research, National Institutes of Health, HHS) Dated: November 18, 2013. David Clary, Program Analyst, Office of Federal Advisory Committee Policy. [FR Doc. 2013–28003 Filed 11–21–13; 8:45 am] BILLING CODE 4140–01–P PO 00000 Frm 00052 Fmt 4703 Sfmt 4703 Number of responses per respondent 1 1 1 Average burden per response (in hours) Total annual burden hour 1 1 1 12 6 12 DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Human Genome Research Institute; Notice of Closed Meeting Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), notice is hereby given of a meeting of the Board of Scientific Counselors, National Human Genome Research Institute. The meeting will be closed to the public as indicated below in accordance with the provisions set forth in section 552b(c)(6), Title 5 U.S.C., as amended for the review, discussion, and evaluation of individual intramural programs and projects conducted by the NATIONAL HUMAN GENOME RESEARCH INSTITUTE, including consideration of personnel qualifications and performance, and the competence of individual investigators, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: Board of Scientific Counselors, National Human Genome Research Institute. Date: December 11–13, 2013. Time: 6:00 p.m. to 1:00 p.m. Agenda: To review and evaluate personal qualifications and performance, and competence of individual investigators. Place: National Institutes of Health, Building 45, Room D, 9000 Rockville Pike, Rockville, MD 20892. Contact Person: Monica Berger, Executive Secretary, Office of the Scientific Director, National Human Genome Research Institute, 50 South Drive, Bldg. 50, Rm. 5222, E:\FR\FM\22NON1.SGM 22NON1

Agencies

[Federal Register Volume 78, Number 226 (Friday, November 22, 2013)]
[Notices]
[Pages 70062-70063]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-27965]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Proposed Collection; 60-Day Comment Request: Clearance for 
Surveys of Customers and Partners of the Office of Extramural Research 
of the National Institutes of Health

SUMMARY: In compliance with the requirement of Section 3506(c)(2)(A) of 
the Paperwork Reduction Act of 1995, for opportunity for public comment 
on proposed data collection projects, the Office of Extramural Research 
(OER), the National Institutes of Health (NIH) will publish periodic 
summaries of proposed projects to be submitted to the Office of 
Management and Budget (OMB) for review and approval.
    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.
    To submit comments in writing, request more information on the 
proposed project, or to obtain a copy of the data collection plans and 
instruments, contact Dr. Sherry Mills, Director, Office of Extramural 
Programs, OER, NIH, 6705 Rockledge Drive, Suite 350, Bethesda, MD 
20892, or call non-toll-free number (301) 435-2729, or Email your 
request, including your address to: OEPMailbox@mail.nih.gov.
    Comments regarding this information collection are best assured of 
having their full effect if received within 60-days of the date of this 
publication.
    Proposed Collection: Generic Clearance for Surveys of Customers and 
Partners of the Office of Extramural Research of the National 
Institutes of Health--Extension--0925-0627--Office of the Director 
(OD), Office of Extramural Research (OER), Office of Extramural 
Programs (OEP), National Institutes of Health (NIH).
    Need and Use of Information Collection: OER develops, coordinates 
the implementation of, and evaluates NIH-wide policies and procedures 
for the award of extramural funds. To move forward with our initiatives 
to ensure success in accomplishing the NIH mission, input from partners 
and customers is essential. Quality management principles have been 
integrated into OER's culture and these surveys will provide customer 
satisfaction input on various elements of OER's business processes. The 
approximately 14 (10 quantitative and 4 qualitative) customer 
satisfaction surveys that will be conducted under this generic 
clearance will gather and measure customer and partner satisfaction 
with OER processes and operations. The data collected from these 
surveys will provide the feedback to track and gauge satisfaction with 
NIH's statutorily mandated operations and processes. OER/OD/NIH will 
present data and outcomes from these surveys to inform the NIH staff, 
officers, leadership, advisory committees, and other decision-making 
bodies as appropriate. Based on feedback from these stakeholders, OER/
OD/NIH will

[[Page 70063]]

formulate improvement plans and take action when necessary.
    OMB approval is requested for 3 years. There are no costs to 
respondents other than their time. The total estimated annualized 
burden hours are 2,485.

Estimated Annualized Burden Hours

                                               Quantitative Survey
----------------------------------------------------------------------------------------------------------------
                                                                     Number of    Average burden
               Type of respondent                    Number of     responses per   per response    Total annual
                                                    respondents     respondent      (in hours)      burden hour
----------------------------------------------------------------------------------------------------------------
Science professionals, applicants, reviewers,              3,820               1           15/60             955
 Institutional Officials........................
Adult Science Trainees..........................           2,000               1           15/60             500
General Public..................................           4,000               1           15/60           1,000
----------------------------------------------------------------------------------------------------------------


                                               Qualitative Survey
----------------------------------------------------------------------------------------------------------------
                                                                     Number of    Average burden
               Type of respondent                    Number of     responses per   per response    Total annual
                                                    respondents     respondent      (in hours)      burden hour
----------------------------------------------------------------------------------------------------------------
Science professionals, applicants, reviewers,                 12               1               1              12
 Institutional Officials........................
Adult Science Trainees..........................               6               1               1               6
General Public..................................              12               1               1              12
----------------------------------------------------------------------------------------------------------------


    Dated: November 13, 2013.
Seleda Perryman,
Chief, Project Clearance Officer, Office of Policy for Extramural 
Research Administration, National Institutes of Health.
[FR Doc. 2013-27965 Filed 11-21-13; 8:45 am]
BILLING CODE 4140-01-P