Advisory Committee on Infant Mortality; Notice of Meeting, 5689 [05-2102]

Download as PDF Federal Register / Vol. 70, No. 22 / Thursday, February 3, 2005 / Notices (21 CFR 10.205), representatives of the electronic media may be permitted, subject to certain limitations, to videotape, film, or otherwise record FDA’s public administrative proceedings, including presentations by participants. The hearing will be transcribed as stipulated in § 15.30(b). The transcript will be available on the Internet at http://www.fda.gov/ohrms/ dockets, and orders for copies of the transcript can be placed at the meeting or through the Division of Dockets Management (see ADDRESSES). Any handicapped persons requiring special accommodations to attend the hearing should direct those needs to the contact person (see FOR FURTHER INFORMATION CONTACT). To the extent that the conditions for the hearing, as described in this notice, conflict with any provisions set out in part 15, this notice acts as a waiver of these provisions as specified in § 15.30(h). IV. Comments Interested persons may submit to the Division of Dockets Management (see ADDRESSES) written or electronic notices of participation and comments for consideration at the hearing (see DATES). Submit a single copy of written or electronic notices of participation and comments, or two paper copies of any mailed notices of participation and comments, except that individuals may submit one copy. Comments are to be identified with the docket number found in brackets in the heading of this document. Received comments may be seen in the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday. Dated: January 28, 2005. Jeffrey Shuren, Assistant Commissioner for Policy. [FR Doc. 05–2094 Filed 1–31–05; 3:37 pm] BILLING CODE 4160–01–S DEPARTMENT OF HEALTH AND HUMAN SERVICES Health Resources and Services Administration Advisory Committee on Infant Mortality; Notice of Meeting In accordance with section 10(a)(2) of the Federal Advisory Committee Act (Pub. L. 92–463), notice is hereby given of the following meeting: Name: Advisory Committee on Infant Mortality (ACIM). Dates and Times: March 1, 2005, 9 a.m.–5 p.m. March 2, 2005, 8:30 a.m.– 3 p.m. VerDate jul<14>2003 19:18 Feb 02, 2005 Jkt 205001 Place: Sheraton National Hotel, 900 South Orme Street, Arlington, Virginia 22204, (703) 521–1900. Status: The meeting is open to the public with attendance limited to space availability. Purpose: The Committee provides advice and recommendations to the Secretary of Health and Human Services on the following: Department programs that are directed at reducing infant mortality and improving the health status of pregnant women and infants; factors affecting the continuum of care with respect to maternal and child health care, including outcomes following childbirth; strategies to coordinate the variety of Federal, State, local and private programs and efforts that are designed to deal with the health and social problems impacting on infant mortality; and the implementation of the Healthy Start program and Healthy People 2010 infant mortality objectives. Agenda: Topics that will be discussed include the following: Improving Perinatal Data; Neonatal Intensive Care and Ethical Issues; and Provider Reimbursement Issues. Substantial time will be spent in small group and full Committee discussions aimed at formulating the ACIM issues agenda. Proposed agenda items are subject to change as priorities indicate. Time will be provided for public comments limited to five minutes each; comments are to be submitted no later than February 15, 2005. FOR FURTHER INFORMATION CONTACT: Anyone requiring information regarding the Committee should contact Peter C. van Dyck, M.D., M.P.H., Executive Secretary, ACIM, Health Resources and Services Administration (HRSA), Room 18–05, Parklawn Building, 5600 Fishers Lane, Rockville, MD 20857, Telephone: (301) 443–2170. Individuals who are submitting public comments or who have questions regarding the meeting should contact Ann M. Koontz, C.N.M., Dr. P.H., HRSA, Maternal and Child Health Bureau, telephone: (301) 443–6327, e-mail: akoontz@hrsa.gov. Dated: January 31, 2005. Steven A. Pelovitz, Associate Administrator for Administration and Financial Management. [FR Doc. 05–2102 Filed 2–2–05; 8:45 am] BILLING CODE 4165–15–P PO 00000 Frm 00089 Fmt 4703 Sfmt 4703 5689 DEPARTMENT OF HEALTH AND HUMAN SERVICES Substance Abuse and Mental Health Services Administration Current List of Laboratories Which Meet Minimum Standards To Engage in Urine Drug Testing for Federal Agencies Substance Abuse and Mental Health Services Administration, HHS. ACTION: Notice. AGENCY: SUMMARY: The Department of Health and Human Services (HHS) notifies Federal agencies of the laboratories currently certified to meet the standards of Subpart C of the Mandatory Guidelines for Federal Workplace Drug Testing Programs (Mandatory Guidelines). The Mandatory Guidelines were first published in the Federal Register on April 11, 1988 (53 FR 11970), and subsequently revised in the Federal Register on June 9, 1994 (59 FR 29908), on September 30, 1997 (62 FR 51118), and on April 13, 2004 (69 FR 19644). A notice listing all currently certified laboratories is published in the Federal Register during the first week of each month. If any laboratory’s certification is suspended or revoked, the laboratory will be omitted from subsequent lists until such time as it is restored to full certification under the Mandatory Guidelines. If any laboratory has withdrawn from the HHS National Laboratory Certification Program (NLCP) during the past month, it will be listed at the end, and will be omitted from the monthly listing thereafter. This notice is also available on the Internet at http://workplace.samhsa.gov and http://www.drugfreeworkplace.gov. FOR FURTHER INFORMATION CONTACT: Mrs. Giselle Hersh or Dr. Walter Vogl, Division of Workplace Programs, SAMHSA/CSAP, Room 2–1035, 1 Choke Cherry Road, Rockville, Maryland 20857; (240) 276–2600 (voice), (240) 276–2610 (fax). SUPPLEMENTARY INFORMATION: The Mandatory Guidelines were developed in accordance with Executive Order 12564 and section 503 of Pub. L. 100– 71. Subpart C of the Mandatory Guidelines, ‘‘Certification of Laboratories Engaged in Urine Drug Testing for Federal Agencies,’’ sets strict standards that laboratories must meet in order to conduct drug and specimen validity tests on urine specimens for Federal agencies. To become certified, an applicant laboratory must undergo three rounds of performance testing plus an on-site inspection. To maintain that E:\FR\FM\03FEN1.SGM 03FEN1

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[Federal Register Volume 70, Number 22 (Thursday, February 3, 2005)]
[Notices]
[Page 5689]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-2102]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Health Resources and Services Administration


Advisory Committee on Infant Mortality; Notice of Meeting

    In accordance with section 10(a)(2) of the Federal Advisory 
Committee Act (Pub. L. 92-463), notice is hereby given of the following 
meeting:
    Name: Advisory Committee on Infant Mortality (ACIM).
    Dates and Times: March 1, 2005, 9 a.m.-5 p.m. March 2, 2005, 8:30 
a.m.-3 p.m.
    Place: Sheraton National Hotel, 900 South Orme Street, Arlington, 
Virginia 22204, (703) 521-1900.
    Status: The meeting is open to the public with attendance limited 
to space availability.
    Purpose: The Committee provides advice and recommendations to the 
Secretary of Health and Human Services on the following: Department 
programs that are directed at reducing infant mortality and improving 
the health status of pregnant women and infants; factors affecting the 
continuum of care with respect to maternal and child health care, 
including outcomes following childbirth; strategies to coordinate the 
variety of Federal, State, local and private programs and efforts that 
are designed to deal with the health and social problems impacting on 
infant mortality; and the implementation of the Healthy Start program 
and Healthy People 2010 infant mortality objectives.
    Agenda: Topics that will be discussed include the following: 
Improving Perinatal Data; Neonatal Intensive Care and Ethical Issues; 
and Provider Reimbursement Issues. Substantial time will be spent in 
small group and full Committee discussions aimed at formulating the 
ACIM issues agenda. Proposed agenda items are subject to change as 
priorities indicate.
    Time will be provided for public comments limited to five minutes 
each; comments are to be submitted no later than February 15, 2005.

FOR FURTHER INFORMATION CONTACT: Anyone requiring information regarding 
the Committee should contact Peter C. van Dyck, M.D., M.P.H., Executive 
Secretary, ACIM, Health Resources and Services Administration (HRSA), 
Room 18-05, Parklawn Building, 5600 Fishers Lane, Rockville, MD 20857, 
Telephone: (301) 443-2170.
    Individuals who are submitting public comments or who have 
questions regarding the meeting should contact Ann M. Koontz, C.N.M., 
Dr. P.H., HRSA, Maternal and Child Health Bureau, telephone: (301) 443-
6327, e-mail: akoontz@hrsa.gov.

    Dated: January 31, 2005.
Steven A. Pelovitz,
Associate Administrator for Administration and Financial Management.
[FR Doc. 05-2102 Filed 2-2-05; 8:45 am]
BILLING CODE 4165-15-P