National Institute of Arthritis and Musculoskeletal and Skin Diseases; Closed Meeting, 17679-17680 [2013-06571]

Download as PDF Federal Register / Vol. 78, No. 56 / Friday, March 22, 2013 / Notices ++ AOA/HFAP’s processes and procedures for monitoring a hospital that is out of compliance with AOA/ HFAP’s program requirements. These monitoring procedures are used only when AOA/HFAP identifies noncompliance. If noncompliance is identified through validation reviews or complaint surveys, the state survey agency monitors corrections as specified at § 488.7(d). ++ AOA/HFAP’s capacity to report deficiencies to the surveyed facilities and respond to the facility’s plan of correction in a timely manner. ++ AOA/HFAP’s capacity to provide CMS with electronic data and reports necessary for effective validation and assessment of the organization’s survey process. ++ The adequacy of AOA/HFAP’s staff and other resources, and its financial viability. ++ AOA/HFAP’s capacity to adequately fund required surveys. ++ AOA/HFAP’s policies with respect to whether surveys are announced or unannounced. ++ AOA/HFAP’s agreement to provide CMS with a copy of the most current accreditation survey together with any other information related to the survey as CMS may require (including corrective action plans). IV. Collection of Information Requirements This document does not impose information collection and recordkeeping requirements. Consequently, it need not be reviewed by the Office of Management and Budget under the authority of the Paperwork Reduction Act of 1995 (44 U.S.C. 35). srobinson on DSK4SPTVN1PROD with NOTICES V. Response to Public Comments Because of the large number of public comments we normally receive on Federal Register documents, we are not able to acknowledge or respond to them individually. We will consider all comments we receive by the date and time specified in the DATES section of this preamble, and, when we proceed with a subsequent document, we will respond to the comments in the preamble to that document. Upon completion of our evaluation, including evaluation of comments received as a result of this notice, we will publish a final notice in the Federal Register announcing the result of our evaluation. (Catalog of Federal Domestic Assistance Program No. 93.778, Medical Assistance Program; No. 93.773 Medicare—Hospital Insurance Program; and No. 93.774, VerDate Mar<15>2010 18:27 Mar 21, 2013 Jkt 229001 Medicare—Supplementary Medical Insurance Program) Dated: March 5, 2013. Marilyn Tavenner, Administrator, Centers for Medicare & Medicaid Services. [FR Doc. 2013–06640 Filed 3–21–13; 8:45 am] BILLING CODE 4120–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Implementation of the Updated American Veterinary Medical Association Guidelines for the Euthanasia of Animals: 2013 Edition SUMMARY: The National Institutes of Health (NIH) is providing guidance to Public Health Service (PHS) awardee institutions on implementation of the American Veterinary Medical Association (AVMA) Guidelines for the Euthanasia of Animals: 2013 Edition (Guidelines). The NIH is seeking input from the public on any concerns they may have regarding the updated Guidelines. DATES: Public concerns regarding the updated AVMA Guidelines for the Euthanasia of Animals: 2013 Edition must be submitted electronically at http://grants.nih.gov/grants/olaw/ 2013avmaguidelines_comments/ add.cfm?ID=32 by May 31, 2013, in order to be considered. FOR FURTHER INFORMATION CONTACT: Office of Laboratory Animal Welfare, Office of Extramural Research, NIH, RKL1, Suite 360, 6705 Rockledge Drive, Bethesda, MD 20892–7982; phone 301– 496–7163; email olaw@od.nih.gov. SUPPLEMENTARY INFORMATION: I. Background The NIH Office of Laboratory Animal Welfare (OLAW) oversees PHS-funded animal activities by the authority of the Health Research Extension Act of 1985 (http://grants.nih.gov/grants/olaw/ references/hrea1985.htm) and the PHS Policy on Humane Care and Use of Laboratory Animals (PHS Policy; http://grants.nih.gov/grants/olaw/ references/phspol.htm). The PHS Policy IV.C.1.G. (http://grants.nih.gov/grants/ olaw/references/phspol.htm# ReviewofPHS-ConductedorSupported ResearchProjects) requires that Institutional Animal Care and Use Committees (IACUCs) reviewing PHSconducted or -supported research projects, determine if methods of euthanasia used in projects will be consistent with the recommendations of the AVMA Panel on Euthanasia, unless PO 00000 Frm 00053 Fmt 4703 Sfmt 4703 17679 a deviation is justified for scientific reasons in writing by the investigator. PHS-Assured institutions are encouraged to begin using the 2013 Guidelines as soon as possible when reviewing research projects, and full implementation is expected after September 1, 2013. Previously approved projects undergoing continuing review according to PHS Policy IV.C.5. (http://grants.nih.gov/grants/olaw/ references/phspol.htm#ReviewofPHSConductedorSupportedResearch Projects), which requires a complete de novo review at least once every 3 years, must be reviewed using the 2013 Guidelines after September 1, 2013. II. Electronic Access The AVMA has issued and posted an update to the 2007 Guidelines on Euthanasia with a new title, AVMA Guidelines for the Euthanasia of Animals: 2013 Edition, available at https://www.avma.org/KB/Policies/ Documents/euthanasia.pdf (PDF). Dated: March 14, 2013. Francis S. Collins, Director, National Institutes of Health. [FR Doc. 2013–06661 Filed 3–21–13; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute of Arthritis and Musculoskeletal and Skin Diseases; 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 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 Arthritis and Musculoskeletal and Skin Diseases Special Emphasis Panel; NIAMS Clinical Trial Outcome Development. Date: March 29, 2013. Time: 8:00 a.m. to 5:30 p.m. Agenda: To review and evaluate grant applications. Place: Hilton Washington/Rockville, 1750 Rockville Pike, Rockville, MD 20852. E:\FR\FM\22MRN1.SGM 22MRN1 17680 Federal Register / Vol. 78, No. 56 / Friday, March 22, 2013 / Notices Contact Person: Xincheng Zheng, Ph.D., M.D., Scientific Review Officer, Scientific Review Branch, National Institute of Arthritis, Musculoskeletal and Skin Diseases, NIH, 6701 Democracy Boulevard, Suite 800, Bethesda, MD 20892, 301–594–4953, xincheng.zheng@nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.846, Arthritis, Musculoskeletal and Skin Diseases Research, National Institutes of Health, HHS) Dated: March 18, 2013. Carolyn Baum, Program Analyst, Office of Federal Advisory Committee Policy. [FR Doc. 2013–06571 Filed 3–21–13; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute on Alcohol Abuse and Alcoholism; Closed Meeting srobinson on DSK4SPTVN1PROD 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: National Institute on Alcohol Abuse and Alcoholism, Special Emphasis Panel, NIAAA Member Conflict Applications. Date: April 4, 2013. Time: 11:00 a.m. to 3:00 p.m. Agenda: To review and evaluate grant applications. Place: 5635 Fishers Lane, Rockville, MD 20852 (Telephone Conference Call). Contact Person: Ranga Srinivas, Ph.D., Chief, Extramural Project Review Branch EPRB, NIAAA, National Institutes of Health, 5365 Fishers Lane, Room 2085, Rockville, MD 20852 (301) 451–2067 srinivar@mail.nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.273, Alcohol Research Programs; National Institutes of Health, HHS) Dated: March 18, 2013. Carolyn A. Baum, Program Analyst, Office of Federal Advisory Committee Policy. [FR Doc. 2013–06572 Filed 3–21–13; 8:45 am] BILLING CODE 4140–01–P VerDate Mar<15>2010 18:27 Mar 21, 2013 Jkt 229001 DEPARTMENT OF HOMELAND SECURITY [Docket No. DHS–2012–0061] Information Collection Request; Chemical Facility Anti-Terrorism Standards Personnel Surety Program National Protection and Programs Directorate, DHS. ACTION: 60-Day notice and request for comments; New Information Collection Request: 1670—NEW. AGENCY: SUMMARY: The Department of Homeland Security (DHS), National Protection and Programs Directorate (NPPD), Office of Infrastructure Protection (IP), Infrastructure Security Compliance Division (ISCD) will submit the following Information Collection Request (ICR) to the Office of Management and Budget (OMB) for review and clearance in accordance with the Paperwork Reduction Act (PRA) of 1995 (Pub. L. 104–13, 44 U.S.C. Chapter 35). This is a new information collection and follows the withdrawal of a previous ICR on the same topic.1 The purpose of this notice is to solicit comments during a 60-day public comment period prior to the submission of this ICR to OMB. The submission describes the nature of the information collection, the categories of respondents, the estimated burden (in hours), and the estimated burden cost necessary to implement the Chemical Facility Anti-Terrorism Standards (CFATS) Personnel Surety Program pursuant to 6 CFR 27.230(a)(12)(iv). DATES: Comments are encouraged and will be accepted until May 21, 2013. This process is conducted in accordance with 5 CFR 1320.8. ADDRESSES: Interested persons are invited to submit comments on the proposed information collection through the Federal eRulemaking Portal at http://www.regulations.gov. All 1 A 60-day public notice for comments was published in the Federal Register on June 10, 2009. See 74 FR 27555. Comments submitted by the public may be found on http://www.regulations.gov under Docket ID DHS–2009–0026. The Department’s responses were included in a Paperwork Reduction Act (PRA) 30-day Federal Register notice. The 30-day public notice for comments was published in the Federal Register on April 13, 2010. See 75 FR 18850. Comments submitted by the public may be found on http:// www.regulations.gov under Docket ID DHS–2009– 0026. The Department’s responses were published in a separate Federal Register notice on June 14, 2011. See 76 FR 34720. Concurrently with publication of the June 14, 2011 Federal Register notice, the Department submitted an Information Collection Request about the CFATS Personnel Surety Program to OMB. See http:// www.reginfo.gov/public/do/ PRAViewICR?ref_nbr=201105-1670-002. In July 2012, the Department withdrew that ICR. PO 00000 Frm 00054 Fmt 4703 Sfmt 4703 submissions received must include the words ‘‘Department of Homeland Security’’ and the docket number DHS– 2012–0061. Except as provided below, comments received will be posted without alteration at http:// www.regulations.gov, including any personal information provided. Comments that include trade secrets, confidential commercial or financial information, Chemical-terrorism Vulnerability Information (CVI),2 Sensitive Security Information (SSI),3 or Protected Critical Infrastructure Information (PCII) 4 should not be submitted to the public regulatory docket. Please submit such comments separately from other comments in response to this notice. Comments containing trade secrets, confidential commercial or financial information, CVI, SSI, or PCII should be appropriately marked and packaged in accordance with applicable requirements and submitted by mail to the DHS/NPPD/IP/ISCD CFATS Program Manager at the Department of Homeland Security, 245 Murray Lane, SW., Mail Stop 0610, Arlington, VA 20528–0610. Comments must be identified by docket number DHS– 2012–0061. Table of Contents I. Supplementary Information • Summary of Options Available to HighRisk Chemical Facilities To Comply With RBPS 12(iv) • Scope of This Notice and Commitment To Explore Additional Options in the Future • Who Is Impacted by The CFATS Personnel Surety Program? • What/Who Is the Source of the Information Under Option 1 and Option 2 • CSAT User Roles and Responsibilities • Burden Resulting From the Submission of Duplicate Records About an Affected Individual • Compliance With RBPS 12(iv) and the Potential for Increased Burden To Enter the Restricted Areas or Critical Assets at a High-Risk Chemical Facility • Compliance With RBPS 12(iv) and Infrequent ‘‘Unescorted Visitors’’ • Additional Data Privacy Considerations II. Information Collected About Affected Individuals • Option 1: Collecting Information To Conduct Direct Vetting 2 For more information about CVI see 6 CFR 27.400 and the CVI Procedural Manual at http:// www.dhs.gov/xlibrary/assets/ chemsec_cvi_proceduresmanual.pdf. 3 For more information about SSI see 49 CFR part 1520 and the SSI Program Web page at http:// www.tsa.gov/ssi. 4 For more information about PCII see 6 CFR part 29 and the PCII Program Web page at http:// ww.dhs.gov/pcii. E:\FR\FM\22MRN1.SGM 22MRN1

Agencies

[Federal Register Volume 78, Number 56 (Friday, March 22, 2013)]
[Notices]
[Pages 17679-17680]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-06571]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


National Institute of Arthritis and Musculoskeletal and Skin 
Diseases; 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 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 Arthritis and 
Musculoskeletal and Skin Diseases Special Emphasis Panel; NIAMS 
Clinical Trial Outcome Development.
    Date: March 29, 2013.
    Time: 8:00 a.m. to 5:30 p.m.
    Agenda: To review and evaluate grant applications.
    Place: Hilton Washington/Rockville, 1750 Rockville Pike, 
Rockville, MD 20852.

[[Page 17680]]

    Contact Person: Xincheng Zheng, Ph.D., M.D., Scientific Review 
Officer, Scientific Review Branch, National Institute of Arthritis, 
Musculoskeletal and Skin Diseases, NIH, 6701 Democracy Boulevard, 
Suite 800, Bethesda, MD 20892, 301-594-4953, xincheng.zheng@nih.gov.

(Catalogue of Federal Domestic Assistance Program Nos. 93.846, 
Arthritis, Musculoskeletal and Skin Diseases Research, National 
Institutes of Health, HHS)

    Dated: March 18, 2013.
Carolyn Baum,
Program Analyst, Office of Federal Advisory Committee Policy.
[FR Doc. 2013-06571 Filed 3-21-13; 8:45 am]
BILLING CODE 4140-01-P