Drug Safety and Risk Management Advisory Committee; Amendment of Notice, 2509 [E8-490]

Download as PDF 2509 Federal Register / Vol. 73, No. 10 / Tuesday, January 15, 2008 / Notices Committee Name Tentative Date of Meeting(s) Advisory Committee 10-Digit Information Line Code Molecular and Clinical Genetics Panel May 6–7, November 11–12 3014510231 Neurological Devices Panel March 25–26, June 3–4, September 23–24, November 6– 7 3014512513 Obstetrics and Gynecology Devices Panel April 17–18, June 19–20, August 14–15, October 16–17, December 11–12 3014512524 Ophthalmic Devices Panel February 21–22, May 15–16, September 18–19, November 20–21 3014512396 Orthopedic and Rehabilitation Devices Panel April 21–22, June 16–17, August 18–19, October 20–21, December 8–9 3014512521 Radiological Devices Panel April 15–16, August 12, November 4 3014512526 National Mammography Quality Assurance Advisory Committee October 13–14 3014512397 Technical Electronic Product Radiation Safety Standards Committee October 8 3014512399 July 22, December 2 3014510564 March day to be announced 3014512548 August 12–13 3014512559 CENTER FOR FOOD SAFETY AND APPLIED NUTRITION Food Advisory Committee CENTER FOR VETERINARY MEDICINE Veterinary Medicine Advisory Committee National Center for Toxicological Research (NCTR) Science Advisory Board to NCTR Dated: January 7, 2008. Randall W. Lutter, Deputy Commissioner for Policy. [FR Doc. E8–567 Filed 1–14–08; 8:45 am] Dated: January 7, 2008. Randall W. Lutter, Deputy Commissioner for Policy. [FR Doc. E8–490 Filed 1–14–08; 8:45 am] DEPARTMENT OF HEALTH AND HUMAN SERVICES Fishers Lane, Rockville, MD 20857, 301–827–7001, FAX: 301–827–6776, email: Teresa.Watkins@fda.hhs.gov, or FDA Advisory Committee Information Line, 1–800–741–8138 (301–443–0572 in the Washington DC area), code 3014512535. Please call the Information Line for up-to-date information on this meeting. Food and Drug Administration SUPPLEMENTARY INFORMATION: In the Federal Register of December 11, 2007, FDA announced that a meeting of the Drug Safety and Risk Management Advisory Committee would be held on February 1, 2008. On page 70336, in the second column, the first paragraph of the Agenda portion of document is amended to read as follows: Agenda: The committee will discuss the efficacy and safety of new drug application (NDA) 22–054, INJECTAFER (ferric carboxymaltose injection), Luitpold Pharmaceuticals Inc., used for the treatment of iron deficiency anemia in postpartum patients or iron deficiency anemia in patients with heavy uterine bleeding. This notice is issued under the Federal Advisory Committee Act (5 U.S.C. app. 2) and 21 CFR part 14, relating to the advisory committees. Health Resources and Services Administration BILLING CODE 4160–01–S Drug Safety and Risk Management Advisory Committee; Amendment of Notice AGENCY: Food and Drug Administration, HHS. rwilkins on PROD1PC63 with NOTICES ACTION: Notice. The Food and Drug Administration (FDA) is announcing an amendment to the notice of meeting of the Drug Safety and Risk Management Advisory Committee. This meeting was announced in the Federal Register of December 11, 2007 (72 FR 70336). The amendment is being made to reflect a change in the Agenda portion of the document. There are no other changes. FOR FURTHER INFORMATION CONTACT: Teresa A. Watkins, Center for Drug Evaluation and Research (HFD–21), Food and Drug Administration, 5600 VerDate Aug<31>2005 17:48 Jan 14, 2008 Jkt 214001 PO 00000 Frm 00069 Fmt 4703 Sfmt 4703 BILLING CODE 4160–01–S DEPARTMENT OF HEALTH AND HUMAN SERVICES Notification of Exception to Competition Health Resources and Services Administration, HHS. AGENCY: Notification of Exception to Competition. ACTION: SUMMARY: The Health Resources and Services Administration (HRSA) is issuing a non-competitive program expansion supplement to the National Health Care for the Homeless Council (NHCHC) to provide expanded training and technical assistance to HRSAfunded grantees serving individuals who are homeless. Authority: This activity is under the authority of the Public Health Service Act, section 330(l). E:\FR\FM\15JAN1.SGM 15JAN1

Agencies

[Federal Register Volume 73, Number 10 (Tuesday, January 15, 2008)]
[Notices]
[Page 2509]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-490]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration


Drug Safety and Risk Management Advisory Committee; Amendment of 
Notice

AGENCY:  Food and Drug Administration, HHS.

ACTION:  Notice.

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

    The Food and Drug Administration (FDA) is announcing an amendment 
to the notice of meeting of the Drug Safety and Risk Management 
Advisory Committee. This meeting was announced in the Federal Register 
of December 11, 2007 (72 FR 70336). The amendment is being made to 
reflect a change in the Agenda portion of the document. There are no 
other changes.

FOR FURTHER INFORMATION CONTACT: Teresa A. Watkins, Center for Drug 
Evaluation and Research (HFD-21), Food and Drug Administration, 5600 
Fishers Lane, Rockville, MD 20857, 301-827-7001, FAX: 301-827-6776, e-
mail: Teresa.Watkins@fda.hhs.gov, or FDA Advisory Committee Information 
Line, 1-800-741-8138 (301-443-0572 in the Washington DC area), code 
3014512535. Please call the Information Line for up-to-date information 
on this meeting.

SUPPLEMENTARY INFORMATION: In the Federal Register of December 11, 
2007, FDA announced that a meeting of the Drug Safety and Risk 
Management Advisory Committee would be held on February 1, 2008. On 
page 70336, in the second column, the first paragraph of the Agenda 
portion of document is amended to read as follows:
    Agenda: The committee will discuss the efficacy and safety of new 
drug application (NDA) 22-054, INJECTAFER (ferric carboxymaltose 
injection), Luitpold Pharmaceuticals Inc., used for the treatment of 
iron deficiency anemia in postpartum patients or iron deficiency anemia 
in patients with heavy uterine bleeding.
    This notice is issued under the Federal Advisory Committee Act (5 
U.S.C. app. 2) and 21 CFR part 14, relating to the advisory committees.

    Dated: January 7, 2008.
Randall W. Lutter,
Deputy Commissioner for Policy.
[FR Doc. E8-490 Filed 1-14-08; 8:45 am]
BILLING CODE 4160-01-S
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