National Center for Health Statistics (NCHS), Classifications and Public Health Data Standards Staff, announces the following meeting:, 6403-6404 [2010-2769]

Download as PDF Federal Register / Vol. 75, No. 26 / Tuesday, February 9, 2010 / Notices Cprice-sewell on DSK2BSOYB1PROD with NOTICES Date: February 9, 2010. Closed: 8:30 a.m. to 12 p.m. Agenda: To review and evaluate grant applications and/or proposals. Place: National Institutes of Health, Lawton Chiles International House, Bethesda, MD 20892. Open: 12 p.m. to 3:30 p.m. Agenda: A report of the FIC Director on updates and overviews of new FIC initiatives. Topics to be discussed: New Developments in Chronic Disease Research and Training. Place: National Institutes of Health, Lawton Chiles International House, Bethesda, MD 20892. Contact Person: Robert Eiss, Public Health Advisor, Fogarty International Center, National Institutes of Health, 31 Center Drive, Room B2C02, Bethesda, MD 20892.(301) 496–1415. eissr@mail.nih.gov. This meeting is being published less than 15 days prior to the meeting due to timing limitations imposed by administrative matters. 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. In the interest of security, NIH has instituted stringent procedures for entrance onto the NIH campus. All visitor vehicles, including taxicabs, hotel, and airport shuttles will be inspected before being allowed on campus. Visitors will be asked to show one form of identification (for example, a government-issued photo ID, drivers license, or passport) and to state the purpose of their visit. Information is also available on the Institutes/Center’s home page: https:// www.nih.gov/fic/about/advisory.html, where an agenda and any additional information for the meeting will be posted when available. (Catalogue of Federal Domestic Assistance Program Nos. 93.106, Minority International Research Training Grant in the Biomedical and Behavioral Sciences; 93.154, Special International Postdoctoral Research Program in Acquired Immunodeficiency Syndrome; 93.168, International Cooperative Biodiversity Groups Program; 93.934, Fogarty International Research Collaboration Award; 93.989, Senior International Fellowship Awards Program, National Institutes of Health, HHS) Dated: February 1, 2010. Jennifer Spaeth, Director, Office of Federal Advisory Committee Policy. [FR Doc. 2010–2559 Filed 2–8–10; 8:45 am] BILLING CODE 4140–01–M VerDate Nov<24>2008 14:39 Feb 08, 2010 Jkt 220001 DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention National Center for Health Statistics (NCHS), Classifications and Public Health Data Standards Staff, announces the following meeting: Name: ICD–9–CM Coordination and Maintenance Committee meeting. Time and Date: 9 a.m.–4:30 p.m., March 9–10, 2010. Place: Centers for Medicare and Medicaid Services (CMS) Auditorium, 7500 Security Boulevard, Baltimore, Maryland. Status: Open to the public. Purpose: The ICD–9–CM Coordination and Maintenance (C&M) Committee will hold its first meeting of the 2010 calendar year cycle on Tuesday and Wednesday March 9–10, 2010. The C&M meeting is a public forum for the presentation of proposed modifications to the International Classification of Diseases, Ninth-Revision, Clinical Modification. Matters to be Discussed: Tentative agenda items include: March 9, 2010: ICD–10 updates: GEMs; Freeze update; ICD–10–CM/ICD–10–PCS updates Application of Collagen Based Tissue Sealant Patches Biopsy of Soft Tissue Mass Central Venous Catheter Placement Using Intra-Atrial Electrocardiographic Guidance Circulating Tumor Cell Enumeration, Magnetic Closed Chest Intra-cardiac Mitral Valve Repair Continuous Glucose Monitoring Fat Graft to Breast Insertion of Intracranial Neurostimulator Lead(s) Internal Fixation of Sternum Intralaminar Lumbar Decompression and Laminotomy with Epidurography Intra-operative Fluorescence Vascular Angiography (IFVA) Laparoscopic Hernia Repair without Mesh Thoracoscopic Cardiac Ablation Addenda (procedures) March 10, 2010: Acquired absence of joint Brain death Eaton-Lambert Syndrome E. coli infection Fluency disorders (stuttering) Glaucoma staging H1N1 (Swine flu) Transfusion transmitted infections PO 00000 Frm 00063 Fmt 4703 Sfmt 4703 6403 Uranium exposure Addenda (diagnoses) Contact Person for Additional Information: Amy Blum, Medical Systems Specialist, Classifications and Public Health Data Standards Staff, NCHS, 3311 Toledo Road, Room 2402, Hyattsville, Maryland 20782, e-mail alb8@cdc.gov, telephone 301–458–4106 (diagnosis), Mady Hue, Health Insurance Specialist, Division of Acute Care, CMS, 7500 Security Blvd., Baltimore, Maryland 21244, e-mail marilu.hue@cms.hhs.gov, telephone 410–786–4510 (procedures). Note: CMS and NCHS will no longer be providing paper copies of handouts for the meeting. Electronic copies of all meeting materials will be posted on the CMS and NCHS Web sites prior to the meeting at https://www.cms.hhs.gov/ ICD9ProviderDiagnosticCodes/ 03_meetings.asp#TopOfPage and https:// www.cdc.gov/nchs/icd/ icd9cm_maintenance.htm. Notice: Because of increased security requirements CMS has instituted stringent procedures for entrance into the building by non-government employees. Persons without a government I.D. will need to show an official form of picture I.D., (such as a drivers license), and sign-in at the security desk upon entering the building. Those who wish to attend a specific ICD–9–CM C&M meeting in the CMS auditorium must submit their name and organization for addition to the meeting visitor list. Those wishing to attend the March 9–10, 2010 meeting must submit their name and organization by March 5, 2010 for inclusion on the visitor list. This visitor list will be maintained at the front desk of the CMS building and used by the guards to admit visitors to the meeting. Those who attended previous ICD–9–CM C&M meetings will no longer be automatically added to the visitor list. You must request inclusion of your name prior to each meeting you attend. Register to attend the meeting on-line at: https://www.cms.hhs.gov/ apps/events/. Notice: This is a public meeting. However, because of fire code requirements, should the number of attendants meet the capacity of the room, the meeting will be closed. The Director, Management Analysis and Services Office, has been delegated the authority to sign Federal Register notices pertaining to announcements of meetings and other committee management activities, for both CDC and the Agency for Toxic Substances and Disease Registry. E:\FR\FM\09FEN1.SGM 09FEN1 6404 Federal Register / Vol. 75, No. 26 / Tuesday, February 9, 2010 / Notices Dated: February 1, 2010. Elaine L. Baker, Director, Management Analysis and Services Office, Centers for Disease Control and Prevention. [FR Doc. 2010–2769 Filed 2–8–10; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2008–N–0045] (formerly Docket No. 2004N–0408) Regulatory Site Visit Training Program AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration’s (FDA’s) Center for Biologics Evaluation and Research (CBER) is announcing an invitation for participation in its Regulatory Site Visit Training Program (RSVP). This training program is intended to give CBER regulatory review, compliance, and other relevant staff an opportunity to visit biologics facilities. These visits are intended to allow CBER staff to directly observe routine manufacturing practices and to give CBER staff a better understanding of the biologics industry, including its challenges and operations. The purpose of this notice is to invite biologics facilities to contact CBER for more information if they are interested in participating in this program. DATES: Submit a written or electronic request for participation in this program by March 11, 2010. The request should include a description of your facility relative to products regulated by CBER. Please specify the physical address(es) of the site(s) you are offering. ADDRESSES: If your biologics facility is interested in offering a site visit, you should submit a request to participate in the program to the Division of Dockets Management (HFA–305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. Submit electronic requests to https:// www.regulations.gov. If you previously responded to earlier requests to participate in this program and you continue to be interested in participating, please renew your request through a submission to the Division of Dockets Management. FOR FURTHER INFORMATION CONTACT: Lonnie W. Henderson, Division of Manufacturers Assistance and Training, Center for Biologics Evaluation and Research (HFM–49), Food and Drug Administration, 1401 Rockville Pike, Cprice-sewell on DSK2BSOYB1PROD with NOTICES SUMMARY: VerDate Nov<24>2008 14:39 Feb 08, 2010 Jkt 220001 suite 200N, Rockville, MD 20852–1448, 301–827–2000, FAX: 301–827–3079, email: matt@fda.hhs.gov. SUPPLEMENTARY INFORMATION: I. Background CBER regulates certain biological products including blood and blood products, vaccines, and cellular, tissue, and gene therapies. CBER is committed to advancing the public health through innovative activities that help ensure the safety, effectiveness and availability of biological products to patients. To support this primary goal, CBER has initiated various training and development programs, including programs to further enhance performance of its compliance staff, regulatory review staff, and other relevant staff. CBER seeks to continuously enhance and update review efficiency and quality, and the quality of its regulatory efforts and interactions, by providing CBER staff with a better understanding of the biologics industry and its operations. Further, CBER seeks to enhance: (1) Its understanding of current industry practices, and regulatory impacts and needs; and (2) communication between CBER staff and industry. CBER initiated its RSVP in 2005, and through these annual notices, is requesting those firms that have previously applied and are still interested in participating, to reaffirm their interest, as well as requesting new interested parties to apply. II. RSVP A. Regulatory Site Visits In this program, over a period of time to be agreed upon with the facility, small groups of CBER staff may observe operations of biologics establishments, including for example, blood and tissue establishments. The visits may include packaging facilities, quality control and pathology/toxicology laboratories, and regulatory affairs operations. These visits, or any part of the program, are not intended as a mechanism to inspect, assess, judge, or perform a regulatory function, but are meant to improve mutual understanding and to provide an avenue for open dialogue between the biologics industry and CBER. B. Site Selection All travel expenses associated with the site visits will be the responsibility of CBER. Therefore, selection of potential facilities will be based on the coordination of CBER’s priorities for staff training as well as the limited available resources for this program. In addition to logistical and other resource PO 00000 Frm 00064 Fmt 4703 Sfmt 4703 factors to consider, a key element of site selection is a successful compliance record with FDA or another agency with which we have a memorandum of understanding. If a site visit also involves a visit to a separate physical location of another firm under contract to the applicant, the other firm also needs to agree to participate in the program, as well as have a satisfactory compliance history. III. Requests for Participation Requests are to be identified with the docket number found in the brackets in the heading of this document. Received requests are available for public examination in the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday. Dated: February 4, 2010. Leslie Kux, Acting Assistant Commissioner for Policy. [FR Doc. 2010–2758 Filed 2–8–10; 8:45 am] BILLING CODE 4160–01–S DEPARTMENT OF HOMELAND SECURITY Federal Emergency Management Agency [Internal Agency Docket No. FEMA–3308– EM; Docket ID FEMA–2010–0002] Oklahoma; Emergency and Related Determinations AGENCY: Federal Emergency Management Agency, DHS. ACTION: Notice. SUMMARY: This is a notice of the Presidential declaration of an emergency for the State of Oklahoma (FEMA–3308–EM), dated January 30, 2010, and related determinations. DATES: Effective Date: January 30, 2010. FOR FURTHER INFORMATION CONTACT: Peggy Miller, Disaster Assistance Directorate, Federal Emergency Management Agency, 500 C Street, SW., Washington, DC 20472, (202) 646–3886. SUPPLEMENTARY INFORMATION: Notice is hereby given that, in a letter dated January 30, 2010, the President issued an emergency declaration under the authority of the Robert T. Stafford Disaster Relief and Emergency Assistance Act, 42 U.S.C. 5121–5207 (the Stafford Act), as follows: I have determined that the emergency conditions in certain areas of the State of Oklahoma resulting from a severe winter storm beginning on January 28, 2010, and continuing, are of sufficient severity and magnitude to warrant an emergency declaration under the Robert T. Stafford E:\FR\FM\09FEN1.SGM 09FEN1

Agencies

[Federal Register Volume 75, Number 26 (Tuesday, February 9, 2010)]
[Notices]
[Pages 6403-6404]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-2769]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention


National Center for Health Statistics (NCHS), Classifications and 
Public Health Data Standards Staff, announces the following meeting:

    Name: ICD-9-CM Coordination and Maintenance Committee meeting.
    Time and Date: 9 a.m.-4:30 p.m., March 9-10, 2010.
    Place: Centers for Medicare and Medicaid Services (CMS) Auditorium, 
7500 Security Boulevard, Baltimore, Maryland.
    Status: Open to the public.
    Purpose: The ICD-9-CM Coordination and Maintenance (C&M) Committee 
will hold its first meeting of the 2010 calendar year cycle on Tuesday 
and Wednesday March 9-10, 2010. The C&M meeting is a public forum for 
the presentation of proposed modifications to the International 
Classification of Diseases, Ninth-Revision, Clinical Modification.
    Matters to be Discussed: Tentative agenda items include:

March 9, 2010:
    ICD-10 updates: GEMs; Freeze update; ICD-10-CM/ICD-10-PCS updates
    Application of Collagen Based Tissue Sealant Patches
    Biopsy of Soft Tissue Mass
    Central Venous Catheter Placement Using Intra-Atrial 
Electrocardiographic Guidance
    Circulating Tumor Cell Enumeration, Magnetic
    Closed Chest Intra-cardiac Mitral Valve Repair
    Continuous Glucose Monitoring
    Fat Graft to Breast
    Insertion of Intracranial Neurostimulator Lead(s)
    Internal Fixation of Sternum
    Intralaminar Lumbar Decompression and Laminotomy with Epidurography
    Intra-operative Fluorescence Vascular Angiography (IFVA)
    Laparoscopic Hernia Repair without Mesh
    Thoracoscopic Cardiac Ablation
    Addenda (procedures)
March 10, 2010:
    Acquired absence of joint
    Brain death
    Eaton-Lambert Syndrome
    E. coli infection
    Fluency disorders (stuttering)
    Glaucoma staging
    H1N1 (Swine flu)
    Transfusion transmitted infections
    Uranium exposure
    Addenda (diagnoses)

    Contact Person for Additional Information: Amy Blum, Medical 
Systems Specialist, Classifications and Public Health Data Standards 
Staff, NCHS, 3311 Toledo Road, Room 2402, Hyattsville, Maryland 20782, 
e-mail alb8@cdc.gov, telephone 301-458-4106 (diagnosis), Mady Hue, 
Health Insurance Specialist, Division of Acute Care, CMS, 7500 Security 
Blvd., Baltimore, Maryland 21244, e-mail marilu.hue@cms.hhs.gov, 
telephone 410-786-4510 (procedures). Note: CMS and NCHS will no longer 
be providing paper copies of handouts for the meeting. Electronic 
copies of all meeting materials will be posted on the CMS and NCHS Web 
sites prior to the meeting at https://www.cms.hhs.gov/ICD9ProviderDiagnosticCodes/03_meetings.asp#TopOfPage and https://www.cdc.gov/nchs/icd/icd9cm_maintenance.htm.
    Notice: Because of increased security requirements CMS has 
instituted stringent procedures for entrance into the building by non-
government employees. Persons without a government I.D. will need to 
show an official form of picture I.D., (such as a drivers license), and 
sign-in at the security desk upon entering the building.
    Those who wish to attend a specific ICD-9-CM C&M meeting in the CMS 
auditorium must submit their name and organization for addition to the 
meeting visitor list. Those wishing to attend the March 9-10, 2010 
meeting must submit their name and organization by March 5, 2010 for 
inclusion on the visitor list. This visitor list will be maintained at 
the front desk of the CMS building and used by the guards to admit 
visitors to the meeting. Those who attended previous ICD-9-CM C&M 
meetings will no longer be automatically added to the visitor list. You 
must request inclusion of your name prior to each meeting you attend. 
Register to attend the meeting on-line at: https://www.cms.hhs.gov/apps/events/.
    Notice: This is a public meeting. However, because of fire code 
requirements, should the number of attendants meet the capacity of the 
room, the meeting will be closed.
    The Director, Management Analysis and Services Office, has been 
delegated the authority to sign Federal Register notices pertaining to 
announcements of meetings and other committee management activities, 
for both CDC and the Agency for Toxic Substances and Disease Registry.


[[Page 6404]]


    Dated: February 1, 2010.
Elaine L. Baker,
Director, Management Analysis and Services Office, Centers for Disease 
Control and Prevention.
[FR Doc. 2010-2769 Filed 2-8-10; 8:45 am]
BILLING CODE 4163-18-P
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