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    <title>The Federal Register</title>
    <link>http://thefederalregister.com/b.p/department/DEPARTMENT_OF_HEALTH_AND_HUMAN_SERVICES/2007-11-26/</link>
    <description>Daily Publications of Meetings and Rules Changes for the Federal Government</description>
    <pubDate>Fri, Dec 5 2008 11:00:00 GMT</pubDate>
    <lastBuildDate>Fri, Dec 5 2008 11:00:00 GMT</lastBuildDate>
    <webMaster>info@thefederalregister.com</webMaster>
    <item>
  <title><![CDATA[  Proposed Data Collections Submitted for Public Comment and  Recommendations]]></title>
  <link>http://thefederalregister.com/d.p/2007-11-26-E7-22919</link>
  <description><![CDATA[
</p><p>    In compliance with the requirement of Section 3506(c)(2)(A) of the 
Paperwork Reduction Act of 1995 for opportunity for public comment on 
proposed data collection projects, the Centers for Disease Control and 
Prevention (CDC) will publish periodic summaries of proposed projects. 
To request more information on the proposed projects or to obtain a 
copy of the data collection plans and instruments, call 4046395960 
and send comments to Maryam Daneshvar, Acting CDC Reports Clearance 
Officer, 1600 Clifton Road, MSD 74, Atlanta, GA 30333 or send an e mail to <A HREF="mailto:omb@cdc.gov">omb@cdc.gov</A>.</p><p>    Comments are invited on: (a) Whether the proposed collection of 
information is necessary for the proper performance of the functions of 
the agency, including whether the information shall have practical 
utility; (b) the accuracy of the agency's estimate of the burden of the 
proposed collection of information; (c) ways to enhance the quality, 
utility, and clarity of the information to be collected;<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2007-11-26-E7-22919</guid>
  <pubDate>Mon, Nov 26 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Proposed Data Collections Submitted for Public Comment and  Recommendations]]></title>
  <link>http://thefederalregister.com/d.p/2007-11-26-E7-22920</link>
  <description><![CDATA[
</p><p>    In compliance with the requirement of Section 3506(c)(2)(A) of the 
Paperwork Reduction Act of 1995 for opportunity for public comment on 
proposed data collection projects, the Centers for Disease Control and 
Prevention (CDC) will publish periodic summaries of proposed projects. 
To request more information on the proposed projects or to obtain a 
copy of the data collection plans and instruments, call 4046395960 
and send comments to Maryam I. Daneshvar, CDC Acting Reports Clearance 
Officer, 1600 Clifton Road, MSD74, Atlanta, GA 30333 or send an email  to <A HREF="mailto:omb@cdc.gov">omb@cdc.gov</A>.</p><p>    Comments are invited on: (a) Whether the proposed collection of 
information is necessary for the proper performance of the functions of 
the agency, including whether the information shall have practical 
utility; (b) the accuracy of the agency's estimate of the burden of the  proposed collection of information; (c)<br/> [[Page 65967]]<br/>
ways to enhance the quality, utility, and clarity of the information <script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2007-11-26-E7-22920</guid>
  <pubDate>Mon, Nov 26 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Proposed Data Collections Submitted for Public Comment and  Recommendations]]></title>
  <link>http://thefederalregister.com/d.p/2007-11-26-E7-22930</link>
  <description><![CDATA[
</p><p>    The Centers for Disease Control and Prevention (CDC) publishes a 
list of information collection requests under review by the Office of 
Management and Budget (OMB) in compliance with the Paperwork Reduction 
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call 
the CDC Reports Clearance Officer at (404) 6395960 or send an email 
to <A HREF="mailto:omb@cdc.gov">omb@cdc.gov</A>. Send written comments to CDC Desk Officer, Office of 
Management and Budget, Washington, DC or by fax to (202) 3956974. 
Written comments should be received within 30 days of this notice. Proposed Project</p><p>    Evaluation of the SpanishLanguage Campaign ``Good Morning 
Arthritis, Today You Will Not Defeat Us.''NewNational Center for 
Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for  Disease Control and Prevention (CDC).</p>
<h3>Background and Brief Description</h3>
<p>    Arthritis affects nearly 43 million Americans, or about one in 
every five people, and is the leading cause of disability among adults 
in t<script type="text/javascript">
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]]></description>
  <guid>http://thefederalregister.com/d.p/2007-11-26-E7-22930</guid>
  <pubDate>Mon, Nov 26 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  New Animal Drugs For Use in Animal Feeds; Florfenicol ]]></title>
  <link>http://thefederalregister.com/d.p/2007-11-26-E7-22942</link>
  <description><![CDATA[ The Food and Drug Administration (FDA) is amending the animal 
drug regulations to reflect the approval of a supplemental new animal 
drug application (NADA) filed by ScheringPlough Animal Health Corp. 
The supplemental NADA provides for the use of florfenicol by veterinary 
feed directive (VFD) for the control of mortality in freshwaterreared 
salmonids due to furunculosis associated with Aeromonas salmonicida.
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]]></description>
  <guid>http://thefederalregister.com/d.p/2007-11-26-E7-22942</guid>
  <pubDate>Mon, Nov 26 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Determination That ELOXATIN (Oxaliplatin for Injection), 50 and  100 Milligrams Per Vial, Sterile Lyophilized Powder]]></title>
  <link>http://thefederalregister.com/d.p/2007-11-26-E7-22973</link>
  <description><![CDATA[ The Food and Drug Administration (FDA) has determined that 
ELOXATIN (oxaliplatin for injection), 50 and 100 milligrams (mg) per 
vial, sterile lyophilized powder for injection, was not withdrawn from 
sale for reasons of safety or effectiveness. This determination will 
allow FDA to approve abbreviated new drug applications (ANDAs) for 
oxaliplatin sterile lyophilized powder for injection, 50 and 100 mg/
vial.
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]]></description>
  <guid>http://thefederalregister.com/d.p/2007-11-26-E7-22973</guid>
  <pubDate>Mon, Nov 26 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[
National Toxicology Program (NTP); NTP Interagency Center for the  Evaluation of Alternative Toxicological Methods]]></title>
  <link>http://thefederalregister.com/d.p/2007-11-26-E7-22906</link>
  <description><![CDATA[ NICEATM announces availability of the ICCVAM Test Method 
Evaluation Report: In Vitro Ocular Toxicity Test Methods for 
Identifying Severe Irritants and Corrosives (NIH Publication 074517). 
The report describes four ocular toxicity test methods evaluated by 
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  <guid>http://thefederalregister.com/d.p/2007-11-26-E7-22906</guid>
  <pubDate>Mon, Nov 26 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Proposed Collection; Comment Request; Questionnaire Cognitive  Interview and Pretesting (ARP/DCCPS/NCI)]]></title>
  <link>http://thefederalregister.com/d.p/2007-11-26-E7-22905</link>
  <description><![CDATA[ In compliance with the requirement of section 3506(c)(2)(A) of 
the Paperwork Reduction Act of 1995, for opportunity for public comment 
on proposed data collection projects, the National Cancer Institute 
(NCI), the National Institutes of Health (NIH) will publish periodic 
summaries of proposed projects to be submitted to the Office of  Management and Budget (OMB) for review and approval.</p><p>    Proposed Collection: Title: Questionnaire Cognitive Interview and 
Pretesting. Type of Information Collection Request: NEW. Need and Use 
of Information Collection: The purpose of the data collection is to 
conduct cognitive interviews, focus groups, Pilot household interviews, 
and experimental research in laboratory and field settings, both for 
applied questionnaire evaluation and more basic research on response 
errors in surveys. The most common evaluation method is the cognitive 
interview, in which a questionnaire design specialist interviews a 
volunteer participant. The interviewer administers the draft surve<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2007-11-26-E7-22905</guid>
  <pubDate>Mon, Nov 26 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  NIH Consensus Development Conference: Hydroxyurea Treatment for  Sickle Cell Disease; Notice]]></title>
  <link>http://thefederalregister.com/d.p/2007-11-26-E7-22907</link>
  <description><![CDATA[
</p><p>    Notice is hereby given of the National Institutes of Health (NIH) 
``NIH Consensus Development Conference: Hydroxyurea Treatment for 
Sickle Cell Disease'' to be held February 2527, 2008, in the NIH 
Natcher Conference Center, 45 Center Drive, Bethesda, Maryland 20892. 
The conference will begin at 8:30 a.m. on February 25 and 26, at 9 a.m.  on February 27, and will be open to the public.</p><p>    Sickle cell disease is an inherited blood disorder that affects 
between 50,000 and 75,000 people in the United States. It is most 
common among people whose ancestors come from subSaharan Africa, South 
and Central America, the Middle East, India, and the Mediterranean 
basin. Sickle cell disease occurs when an infant inherits the gene for 
sickle hemoglobin from both parents (Hb SS, or sickle cell anemia) or 
the gene for sickle hemoglobin from one parent and another abnormal 
hemoglobin gene from the other parent. Each year, approximately 2,000 
babies with sickle cell disease are born in the United States. The 
<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2007-11-26-E7-22907</guid>
  <pubDate>Mon, Nov 26 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  National Center on Minority Health and Health Disparities; Notice  of Closed Meeting]]></title>
  <link>http://thefederalregister.com/d.p/2007-11-26-07-5810</link>
  <description><![CDATA[
</p><p>    Pursuant to section 10(d) of the Federal Advisory Committee Act, as 
amended (5 U.S.C. Appendix 2), notice is hereby given of the following  meeting.</p><p>    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.
</p><p>    Name of Committee: National Center on Minority Health and Health 
Disparities Special Emphasis Panel, R13 Conference Grant Review. </p><p>    Date: December 19, 2007.<br/> </p><p>    Time: 8 a.m. to 5 p.m.</p><p>    Agenda: To review and evaluate grant applications.
</p><p>    Place: National Institutes of Health, 6707 Democracy Blvd.,  Bethesda, MD 20892 (Virtual Meeting).</p><p>    Contact Person: Lorrita Watson, PhD.<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2007-11-26-07-5810</guid>
  <pubDate>Mon, Nov 26 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  National Center on Minority Health and Health Disparities; Notice  of Closed Meeting]]></title>
  <link>http://thefederalregister.com/d.p/2007-11-26-07-5811</link>
  <description><![CDATA[
</p><p>    Pursuant to section 10(d) of the Federal Advisory Committee Act, as 
amended (5 U.S.C. Appendix 2), notice is hereby given of the following  meeting.</p><p>    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.
</p><p>    Name of Committee: National Center on Minority Health and Health 
Disparities Special Emphasis Panel, Community Based Participatory  Research (CBPR) Meeting.<br/> </p><p>    Date: December 1618, 2007.<br/> </p><p>    Time: 8 a.m. to 5 p.m.</p><p>    Agenda: To review and evaluate grant applications.
</p><p>    Place: Embassy Suites at the Chevy Chase Pavilion, 4300 Military  Road, NW., Washington DC 20015.</p><p>    Contact <script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2007-11-26-07-5811</guid>
  <pubDate>Mon, Nov 26 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  National Eye Institute; Notice of Closed Meetings ]]></title>
  <link>http://thefederalregister.com/d.p/2007-11-26-07-5813</link>
  <description><![CDATA[
</p><p>    Pursuant to section 10(d) of the Federal Advisory Committee Act, as 
amended (5 U.S.C. Appendix 2), notice is hereby given of the following  meetings.</p><p>    The meetings 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<br/> [[Page 65972]]<br/>
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.</p><p>    Name of Committee: National Eye Institute Special Emphasis  Panel, NEI Clinical Grant Application Review.<br/> </p><p>    Date: December 3, 2007.<br/> </p><p>    Time: 8 a.m. to 5 p.m.</p><p>    Agenda: To review and evaluate grant applications.
</p><p>    Place: Hyatt Regency Bethesda, One Bethesda Metro Center, 7400  Wisconsin Avenue, Bethesda, MD 20814.</p><p>    Contact Person: Houmam H. Araj, PhD., Scie<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2007-11-26-07-5813</guid>
  <pubDate>Mon, Nov 26 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  National Institute of Diabetes and Digestive and Kidney Diseases;  Notice of Closed Meeting]]></title>
  <link>http://thefederalregister.com/d.p/2007-11-26-07-5812</link>
  <description><![CDATA[
</p><p>    Pursuant to section 10(d) of the Federal Advisory Committee Act, as 
amended (5 U.S.C. Appendix 2), notice is hereby given of the following  meeting.</p>
<h3>[[Page 65973]]</h3>
<p>    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.
</p><p>    Name of Committee: National Institute of Diabetes and Digestive 
and Kidney Diseases Special Emphasis Panel, Frequent Hemdialysis  Network (FHN).<br/> </p><p>    Date: January 4, 2008.<br/> </p><p>    Time: 2 p.m. to 5 p.m.</p><p>    Agenda: To review and evaluate grant applications.
</p><p>    Place: National Institutes of Health, Two Democracy Plaza, 6707 
Democracy Boulevard, Bethesda, MD 20892 (Telep<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2007-11-26-07-5812</guid>
  <pubDate>Mon, Nov 26 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  National Institute of Environmental Health Sciences; Notice of  Closed Meeting]]></title>
  <link>http://thefederalregister.com/d.p/2007-11-26-07-5808</link>
  <description><![CDATA[
</p><p>    Pursuant to section 10(d) of the Federal Advisory Committee Act, as 
amended (5 U.S.C. Appendix 2), notice is hereby given of the following  meeting.</p><p>    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.
</p><p>    Name of Committee: National Institute of Environmental Health 
Sciences Special Emphasis Panel, Signaling Pathways in Stages of  Mammary Tumorigenesis.<br/> </p><p>    Date: December 19, 2007.<br/> </p><p>    Time: 1 p.m. to 5 p.m.</p><p>    Agenda: To review and evaluate grant applications.
</p><p>    Place: NIEHS/National Institutes of Health, Building 4401, East 
Campus, 79 T.W. Alexander Drive, Research Triangle Pa<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2007-11-26-07-5808</guid>
  <pubDate>Mon, Nov 26 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  National Institute of Mental Health; Notice of Closed Meeting]]></title>
  <link>http://thefederalregister.com/d.p/2007-11-26-07-5809</link>
  <description><![CDATA[
</p><p>    Pursuant to section 10(d) of the Federal Advisory Committee Act, as 
amended (5 U.S.C. Appendix 2), notice is hereby given of the following  meeting.</p><p>    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.
</p><p>    Name of Committee: National Institute of Mental Health Special  Emphasis Panel, MLSCN HTS ASSAY.<br/> </p><p>    Date: December 14, 2007.<br/> </p><p>    Time: 8 a.m. to 5 p.m.</p><p>    Agenda: To review and evaluate grant applications.
</p><p>    Place: St. Gregory Hotel, 2033 M Street, NW., Washington, DC  20036.</p><p>    Contact Person: Yong Yao, PhD., Scientific Review Administrator, 
Division of Extramural Activities,<script type="text/javascript">
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]]></description>
  <guid>http://thefederalregister.com/d.p/2007-11-26-07-5809</guid>
  <pubDate>Mon, Nov 26 2007 11:00:00 GMT</pubDate>
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<item>
  <title><![CDATA[  Office of the Director, National Institutes of Health; Amended  Notice of Meeting]]></title>
  <link>http://thefederalregister.com/d.p/2007-11-26-07-5814</link>
  <description><![CDATA[
</p><p>    Notice is hereby given of a change in the meeting of the 
Recombinant DNA Advisory Committee, December 3, 2007, 8 a.m. to 
December 5, 2007, 10:30 a.m., National Institutes of Health, Building 
31, Floor 6C, 31 Center Drive, Conference Room 10, Bethesda, MD, 20892, 
which was published in the Federal Register on November 13, 2007, 72 FR  218 page 63917.</p><p>    On December 4, 2007, the Recombinant DNA Advisory Committee meeting 
will be held from 8 a.m. to 11:30 a.m. and begin again at 2:30 p.m. to 
5:30 p.m. instead of meeting from 8 a.m. to 3 p.m. The meeting is open  to the public.<br/> </p><p>    Dated: November 15, 2007.<br/> Jennifer Spaeth,<br/> Director, Office of Federal Advisory Committee Policy.<br/> [FR Doc. 075814 Filed 112307; 8:45 am]<br/>
BILLING CODE 414001M
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  <guid>http://thefederalregister.com/d.p/2007-11-26-07-5814</guid>
  <pubDate>Mon, Nov 26 2007 11:00:00 GMT</pubDate>
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