Advisory Committees; Tentative Schedule of Meetings for 2009, 1690-1692 [E9-451]

Download as PDF 1690 Federal Register / Vol. 74, No. 8 / Tuesday, January 13, 2009 / Notices The agenda is subject to change as priorities dictate. In the event an individual cannot attend, written comments may be submitted. Any written comments received will be provided at the meeting and should be submitted to the contact person below well in advance of the meeting. Contact Person for More Information: Theodore Katz, Executive Secretary, NIOSH, CDC, 1600 Clifton Road, Mailstop E–20, Atlanta, Georgia 30333, Telephone (513) 533–6800, Toll Free 1 (800) CDC–INFO, email ocas@cdc.gov. 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. Dated: January 7, 2009. Elaine L. Baker, Director, Management Analysis and Services Office, Centers for Disease Control and Prevention. [FR Doc. E9–524 Filed 1–12–09; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Comment Request Title: Child Care Quarterly Case Record Report—ACF–801. OMB No.: 0970–0167. Description: Section 658K of the Child Care and Development Block Grant Act of 1990 (Pub. L. 101–508, 42 U.S.C. 9858) requires that States and Territories submit monthly case-level data on the children and families receiving direct services under the Child Care and Development Fund. The implementing regulations for the statutorily required reporting are at 45 CFR 98.70. Case-level reports, submitted quarterly or monthly (at grantee option), include monthly sample or full population case-level data. The data elements to be included in these reports are represented in the ACF–801. ACF uses disaggregate data to determine program and participant characteristics as well as costs and levels of child care services provided. This provides ACF with the information necessary to make reports to Congress, address national child care needs, offer technical assistance to grantees, meet performance measures, and conduct research. Consistent with the statute and regulations, ACF requests extension of the ACF–801. With this extension, ACF is proposing several changes and clarifications to the reporting requirements and instructions. Respondents: States, the District of Columbia, and Territories including Puerto Rico, Guam, the Virgin Islands, American Samoa, and the Northern Mariana Islands. ANNUAL BURDEN ESTIMATES Number of respondents Instrument ACF–801 .......................................................................................................................................... Estimated Total Annual Burden Hours: 4,480 Additional Information: Copies of the proposed collection may be obtained by writing to the Administration for Children and Families, Office of Administration, Office of Information Services, 370 L’Enfant Promenade, SW., Washington, DC 20447, Attn: ACF Reports Clearance Officer. All requests should be identified by the title of the information collection. E-mail address: infocollection@acf.hhs.gov. OMB Comment: OMB is required to make a decision concerning the collection of information between 30 and 60 days after publication of this document in the Federal Register. Therefore, a comment is best assured of having its full effect if OMB receives it within 30 days of publication. Written comments and recommendations for the proposed information collection should be sent directly to the following: Office of Management and Budget, Paperwork Reduction Project, Fax: 202–395–6974, Attn: Desk Officer for the Administration for Children and Families. VerDate Nov<24>2008 19:10 Jan 12, 2009 Jkt 217001 Dated: January 8, 2009. Janean Chambers, Reports Clearance Officer. [FR Doc. E9–447 Filed 1–12–09; 8:45 am] BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2008–N–0038] Advisory Committees; Tentative Schedule of Meetings for 2009 AGENCY: Food and Drug Administration, HHS. ACTION: Notice. SUMMARY: The Food and Drug Administration (FDA) is announcing a tentative schedule of forthcoming meetings of its public advisory committees for 2009. During 1991, at the request of the Commissioner of Food and Drugs (the Commissioner), the Institute of Medicine (the IOM) conducted a study of the use of FDA’s advisory committees. In its final report, one of the IOM’s recommendations was for the agency to publish an annual PO 00000 Frm 00029 Fmt 4703 Sfmt 4703 Number of responses per respondent Average burden hours per response Total burden hours 4 20 4,480 56 tentative schedule of its meetings in the Federal Register. This publication implements the IOM’s recommendation. FOR FURTHER INFORMATION CONTACT: Theresa L. Green, Advisory Committee Oversight and Management Staff (HF– 4), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301–827–1220. SUPPLEMENTARY INFORMATION: The IOM, at the request of the Commissioner, undertook a study of the use of the FDA’s advisory committees. In its final report in 1992, one of the IOM’s recommendations was for FDA to adopt a policy of publishing an advance yearly schedule of its upcoming public advisory committee meetings in the Federal Register; FDA has implemented this recommendation. The annual publication of tentatively scheduled advisory committee meetings will provide both advisory committee members and the public with the opportunity, in advance, to schedule attendance at FDA’s upcoming advisory committee meetings. Because the schedule is tentative, amendments to this notice will not be published in the Federal Register. However, changes to the schedule will be posted on the FDA E:\FR\FM\13JAN1.SGM 13JAN1 Federal Register / Vol. 74, No. 8 / Tuesday, January 13, 2009 / Notices advisory committees’ Internet site located at https://www.fda.gov/oc/ advisory/default.htm. FDA will continue to publish a Federal Register notice 15 days in advance of each upcoming advisory committee meeting, to announce the meeting (21 CFR 14.20). The following list announces FDA’s tentatively scheduled advisory committee meetings for 2009. You may Committee Name 1691 also obtain up-to-date information by calling the Advisory Committee Information Line, 1–800–741–8138 (301–443–0572 in the Washington, DC area). Advisory Committee 10-Digit Information Line Code Tentative Date of Meeting(s) OFFICE OF THE COMMISSIONER Pediatric Advisory Committee March 23–24, June 22–23, September 21–22, December 7–8 8732310001 Risk Communication Advisory Committee February 26–27, April 30–May 1, August 13–14, November 12–13 8732112560 Science Board to the Food and Drug Administration February 24, May 18, August 17, November 16 3014512603 CENTER FOR BIOLOGICS EVALUATION AND RESEARCH Allergenic Products Advisory Committee March 5, October 22 3014512388 Blood Products Advisory Committee January 9, April 1, July 20–21, November 16–17 3014519516 Cellular, Tissue and Gene Therapies Advisory Committee May 14–15, November 5–6 3014512389 Transmissible Spongiform Encephalopathies Advisory Committee To be announced 3014512392 Vaccines and Related Biological Products Advisory Committee February 18–19, May 20–21, September 23–24, November 18–19 3014512391 CENTER FOR DRUG EVALUATION AND RESEARCH Anesthetic and Life Support Drugs Advisory Committee January 29–30, April dates to be announced 3014512529 Anti-Infective Drugs Advisory Committee To be announced 3014512530 Antiviral Drugs Advisory Committee To be announced 3014512531 Arthritis Advisory Committee March 5, June 16–17, October 27–28 3014512532 Cardiovascular and Renal Drugs Advisory Committee February 3, March 18–19, July 28–29, December 7–8 3014512533 Dermatologic and Ophthalmic Drugs Advisory Committee To be announced 3014512534 Drug Safety and Risk Management Advisory Committee January 30, April dates to be announced 3014512535 Endocrinologic and Metabolic Drugs Advisory Committee April 2–3 3014512536 Gastrointestinal Drugs Advisory Committee February 17 3014512538 Nonprescription Drugs Advisory Committee April dates to be announced 3014512541 Oncologic Drugs Advisory Committee February 25, March 24–25, May dates to be announced, July 14–15, September 15–16, December 16–17 3014512542 Peripheral and Central Nervous System Drugs Advisory Committee January 7–8 3014512543 Pharmaceutical Science and Clinical Pharmacology, Advisory Committee for March dates to be announced 3014512539 Psychopharmacologic Drugs Advisory Committee March 26 3014512544 Pulmonary-Allergy Drugs Advisory Committee February 4 3014512545 Reproductive Health Drugs, Advisory Committee for May and August dates to be announced 3014512537 CENTER FOR DEVICES AND RADIOLOGICAL HEALTH Device Good Manufacturing Practice Advisory Committee April 15, October 5–6 3014512398 Medical Devices Advisory Committee (Comprised of 18 Panels) VerDate Nov<24>2008 19:10 Jan 12, 2009 Jkt 217001 PO 00000 Frm 00030 Fmt 4703 Sfmt 4703 E:\FR\FM\13JAN1.SGM 13JAN1 1692 Federal Register / Vol. 74, No. 8 / Tuesday, January 13, 2009 / Notices Committee Name Advisory Committee 10-Digit Information Line Code Tentative Date of Meeting(s) Anesthesiology and Respiratory Therapy Devices Panel February 5, April 30, July 23, September 17, November 12 3014512624 Circulatory System Devices Panel February 25, May 27, September 24 3014512625 Clinical Chemistry and Clinical Toxicology Devices Panel March 18–19, June 17–18, October 21–22 3014512514 Dental Products Panel February 11, May 6, June 17, September 16, December 9 3014512518 Ear, Nose, and Throat Devices Panel February 24, May 19, August 18, November 17 3014512522 Gastroenterology-Urology Devices Panel March 20, October 15 3014512523 General and Plastic Surgery Devices Panel February 26–27, June 9–10, October 15–16 3014512519 General Hospital and Personal Use Devices Panel March 25–26, July 29–30, October 21–22 3014512520 Hematology and Pathology Devices Panel April 24, July 17, October 23 3014512515 Immunology Devices Panel October 15–16 3014512516 Medical Devices Dispute Resolution Panel Meetings occur as needed 3014510232 Microbiology Devices Panel February 24–25, September 22–23, October 27–28 3014512517 Molecular and Clinical Genetics Panel April 15, October 5–6 3014510231 Neurological Devices Panel February 26–27, May 14–15, September 17–18, December 2–3 3014512513 Obstetrics and Gynecology Devices Panel February 5–6, May 14–15, August 13–14, November 12– 13 3014512524 Ophthalmic Devices Panel February 12–13, May 14–15, September 24–25,November 19–20 3014512396 Orthopaedic and Rehabilitation Devices Panel February 3–4, April 14–15, June 9–10, August 11–12, October 15–16, December 1–2 3014512521 Radiological Devices Panel February 18, May 12, August 4, November 17 3014512526 National Mammography Quality Assurance Advisory Committee November 4–5 3014512397 Technical Electronic Product Radiation Safety Standards Committee No meeting tentatively scheduled for 2009 3014512399 CENTER FOR FOOD SAFETY AND APPLIED NUTRITION Food Advisory Committee May 20–21 3014510564 CENTER FOR VETERINARY MEDICINE Veterinary Medicine Advisory Committee April 14 3014512548 NATIONAL CENTER FOR TOXILOGICAL RESEARCH (NCTR) Science Advisory Board to NCTR November 17–18 3014512559 Dated: December 24, 2008. Randall W. Lutter, Deputy Commissioner for Policy. [FR Doc. E9–451 Filed 1–12–09; 8:45 am] DEPARTMENT OF HEALTH AND HUMAN SERVICES BILLING CODE 4160–01–S [Docket No. FDA–2009–D–0675] Food and Drug Administration Draft Guidance for Industry on Good Importer Practices; Availability AGENCY: Food and Drug Administration, HHS. ACTION: VerDate Nov<24>2008 19:10 Jan 12, 2009 Jkt 217001 PO 00000 Notice. Frm 00031 Fmt 4703 Sfmt 4703 SUMMARY: The Food and Drug Administration (FDA) is announcing on behalf of several members of the Interagency Working Group on Import Safety (agencies) the availability of a draft guidance for industry entitled ‘‘Good Importer Practices.’’ This draft guidance document provides general recommendations to importers on possible practices and procedures they may follow to increase the likelihood the products they import are in E:\FR\FM\13JAN1.SGM 13JAN1

Agencies

[Federal Register Volume 74, Number 8 (Tuesday, January 13, 2009)]
[Notices]
[Pages 1690-1692]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-451]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2008-N-0038]


Advisory Committees; Tentative Schedule of Meetings for 2009

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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

SUMMARY: The Food and Drug Administration (FDA) is announcing a 
tentative schedule of forthcoming meetings of its public advisory 
committees for 2009. During 1991, at the request of the Commissioner of 
Food and Drugs (the Commissioner), the Institute of Medicine (the IOM) 
conducted a study of the use of FDA's advisory committees. In its final 
report, one of the IOM's recommendations was for the agency to publish 
an annual tentative schedule of its meetings in the Federal Register. 
This publication implements the IOM's recommendation.

FOR FURTHER INFORMATION CONTACT: Theresa L. Green, Advisory Committee 
Oversight and Management Staff (HF-4), Food and Drug Administration, 
5600 Fishers Lane, Rockville, MD 20857, 301-827-1220.

SUPPLEMENTARY INFORMATION: The IOM, at the request of the Commissioner, 
undertook a study of the use of the FDA's advisory committees. In its 
final report in 1992, one of the IOM's recommendations was for FDA to 
adopt a policy of publishing an advance yearly schedule of its upcoming 
public advisory committee meetings in the Federal Register; FDA has 
implemented this recommendation. The annual publication of tentatively 
scheduled advisory committee meetings will provide both advisory 
committee members and the public with the opportunity, in advance, to 
schedule attendance at FDA's upcoming advisory committee meetings. 
Because the schedule is tentative, amendments to this notice will not 
be published in the Federal Register. However, changes to the schedule 
will be posted on the FDA

[[Page 1691]]

advisory committees' Internet site located at https://www.fda.gov/oc/
advisory/default.htm. FDA will continue to publish a Federal Register 
notice 15 days in advance of each upcoming advisory committee meeting, 
to announce the meeting (21 CFR 14.20).
    The following list announces FDA's tentatively scheduled advisory 
committee meetings for 2009. You may also obtain up-to-date information 
by calling the Advisory Committee Information Line, 1-800-741-8138 
(301-443-0572 in the Washington, DC area).

------------------------------------------------------------------------
                                                     Advisory Committee
     Committee Name           Tentative Date of     10-Digit Information
                                 Meeting(s)               Line Code
------------------------------------------------------------------------
                       OFFICE OF THE COMMISSIONER
------------------------------------------------------------------------
Pediatric Advisory        March 23-24, June 22-23,            8732310001
 Committee                 September 21-22,
                           December 7-8
------------------------------------------------------------------------
Risk Communication        February 26-27, April 30-           8732112560
 Advisory Committee        May 1, August 13-14,
                           November 12-13
------------------------------------------------------------------------
Science Board to the      February 24, May 18,                3014512603
 Food and Drug             August 17, November 16
 Administration
------------------------------------------------------------------------
              CENTER FOR BIOLOGICS EVALUATION AND RESEARCH
------------------------------------------------------------------------
Allergenic Products       March 5, October 22                 3014512388
 Advisory Committee
------------------------------------------------------------------------
Blood Products Advisory   January 9, April 1, July            3014519516
 Committee                 20-21, November 16-17
------------------------------------------------------------------------
Cellular, Tissue and      May 14-15, November 5-6             3014512389
 Gene Therapies Advisory
 Committee
------------------------------------------------------------------------
Transmissible Spongiform  To be announced                     3014512392
 Encephalopathies
 Advisory Committee
------------------------------------------------------------------------
Vaccines and Related      February 18-19, May 20-             3014512391
 Biological Products       21, September 23-24,
 Advisory Committee        November 18-19
------------------------------------------------------------------------
                 CENTER FOR DRUG EVALUATION AND RESEARCH
------------------------------------------------------------------------
Anesthetic and Life       January 29-30, April                3014512529
 Support Drugs Advisory    dates to be announced
 Committee
------------------------------------------------------------------------
Anti-Infective Drugs      To be announced                     3014512530
 Advisory Committee
------------------------------------------------------------------------
Antiviral Drugs Advisory  To be announced                     3014512531
 Committee
------------------------------------------------------------------------
Arthritis Advisory        March 5, June 16-17,                3014512532
 Committee                 October 27-28
------------------------------------------------------------------------
Cardiovascular and Renal  February 3, March 18-19,            3014512533
 Drugs Advisory            July 28-29, December 7-
 Committee                 8
------------------------------------------------------------------------
Dermatologic and          To be announced                     3014512534
 Ophthalmic Drugs
 Advisory Committee
------------------------------------------------------------------------
Drug Safety and Risk      January 30, April dates             3014512535
 Management Advisory       to be announced
 Committee
------------------------------------------------------------------------
Endocrinologic and        April 2-3                           3014512536
 Metabolic Drugs
 Advisory Committee
------------------------------------------------------------------------
Gastrointestinal Drugs    February 17                         3014512538
 Advisory Committee
------------------------------------------------------------------------
Nonprescription Drugs     April dates to be                   3014512541
 Advisory Committee        announced
------------------------------------------------------------------------
Oncologic Drugs Advisory  February 25, March 24-              3014512542
 Committee                 25, May dates to be
                           announced, July 14-15,
                           September 15-16,
                           December 16-17
------------------------------------------------------------------------
Peripheral and Central    January 7-8                         3014512543
 Nervous System Drugs
 Advisory Committee
------------------------------------------------------------------------
Pharmaceutical Science    March dates to be                   3014512539
 and Clinical              announced
 Pharmacology, Advisory
 Committee for
------------------------------------------------------------------------
Psychopharmacologic       March 26                            3014512544
 Drugs Advisory
 Committee
------------------------------------------------------------------------
Pulmonary-Allergy Drugs   February 4                          3014512545
 Advisory Committee
------------------------------------------------------------------------
Reproductive Health       May and August dates to             3014512537
 Drugs, Advisory           be announced
 Committee for
------------------------------------------------------------------------
               CENTER FOR DEVICES AND RADIOLOGICAL HEALTH
------------------------------------------------------------------------
Device Good               April 15, October 5-6               3014512398
 Manufacturing Practice
 Advisory Committee
------------------------------------------------------------------------
Medical Devices Advisory Committee (Comprised of 18 Panels)
------------------------------------------------------------------------

[[Page 1692]]

 
Anesthesiology and        February 5, April 30,               3014512624
 Respiratory Therapy       July 23, September 17,
 Devices Panel             November 12
------------------------------------------------------------------------
Circulatory System        February 25, May 27,                3014512625
 Devices Panel             September 24
------------------------------------------------------------------------
Clinical Chemistry and    March 18-19, June 17-18,            3014512514
 Clinical Toxicology       October 21-22
 Devices Panel
------------------------------------------------------------------------
Dental Products Panel     February 11, May 6, June            3014512518
                           17, September 16,
                           December 9
------------------------------------------------------------------------
Ear, Nose, and Throat     February 24, May 19,                3014512522
 Devices Panel             August 18, November 17
------------------------------------------------------------------------
Gastroenterology-Urology  March 20, October 15                3014512523
 Devices Panel
------------------------------------------------------------------------
General and Plastic       February 26-27, June 9-             3014512519
 Surgery Devices Panel     10, October 15-16
------------------------------------------------------------------------
General Hospital and      March 25-26, July 29-30,            3014512520
 Personal Use Devices      October 21-22
 Panel
------------------------------------------------------------------------
Hematology and Pathology  April 24, July 17,                  3014512515
 Devices Panel             October 23
------------------------------------------------------------------------
Immunology Devices Panel  October 15-16                       3014512516
------------------------------------------------------------------------
Medical Devices Dispute   Meetings occur as needed            3014510232
 Resolution Panel
------------------------------------------------------------------------
Microbiology Devices      February 24-25,                     3014512517
 Panel                     September 22-23,
                           October 27-28
------------------------------------------------------------------------
Molecular and Clinical    April 15, October 5-6               3014510231
 Genetics Panel
------------------------------------------------------------------------
Neurological Devices      February 26-27, May 14-             3014512513
 Panel                     15, September 17-18,
                           December 2-3
------------------------------------------------------------------------
Obstetrics and            February 5-6, May 14-15,            3014512524
 Gynecology Devices        August 13-14, November
 Panel                     12-13
------------------------------------------------------------------------
Ophthalmic Devices Panel  February 12-13, May 14-             3014512396
                           15, September 24-
                           25,November 19-20
------------------------------------------------------------------------
Orthopaedic and           February 3-4, April 14-             3014512521
 Rehabilitation Devices    15, June 9-10, August
 Panel                     11-12, October 15-16,
                           December 1-2
------------------------------------------------------------------------
Radiological Devices      February 18, May 12,                3014512526
 Panel                     August 4, November 17
------------------------------------------------------------------------
National Mammography      November 4-5                        3014512397
 Quality Assurance
 Advisory Committee
------------------------------------------------------------------------
Technical Electronic      No meeting tentatively              3014512399
 Product Radiation         scheduled for 2009
 Safety Standards
 Committee
------------------------------------------------------------------------
              CENTER FOR FOOD SAFETY AND APPLIED NUTRITION
------------------------------------------------------------------------
Food Advisory Committee   May 20-21                           3014510564
------------------------------------------------------------------------
                     CENTER FOR VETERINARY MEDICINE
------------------------------------------------------------------------
Veterinary Medicine       April 14                            3014512548
 Advisory Committee
------------------------------------------------------------------------
             NATIONAL CENTER FOR TOXILOGICAL RESEARCH (NCTR)
------------------------------------------------------------------------
Science Advisory Board    November 17-18                      3014512559
 to NCTR
------------------------------------------------------------------------


    Dated: December 24, 2008.
Randall W. Lutter,
Deputy Commissioner for Policy.
[FR Doc. E9-451 Filed 1-12-09; 8:45 am]
BILLING CODE 4160-01-S
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