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    <title>The Federal Register</title>
    <link>http://thefederalregister.com/b.p/department/DEPARTMENT_OF_HEALTH_AND_HUMAN_SERVICES/2003-12-05/</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/2003-12-05-03-30257</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 the CDC Reports  Clearance Officer on (404) 4981210.</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; and (d) ways 
to minimize the burden of the collection of information on respondents, 
including through the use of automated collection techniques <script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2003-12-05-03-30257</guid>
  <pubDate>Fri, Dec 5 2003 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  National Center on Birth Defects and Developmental Disabilities]]></title>
  <link>http://thefederalregister.com/d.p/2003-12-05-03-30216</link>
  <description><![CDATA[
</p><p>    Name: Scientific Workshop on Impact of Maternal Thyroid Disease on 
the Developing Fetus: Implications for Diagnosis, Treatment, and  Screening.</p><p>    Times and Dates: 8 a.m.7:30 p.m., January 12, 2004. 8 a.m.4 p.m.,  January 13, 2004.</p><p>    Place: Renaissance Atlanta Hotel Downtown, 590 West Peachtree 
Street, NW., Atlanta, Georgia 303083586, Telephone (404) 8816000.
</p><p>    Status: Open to the public, limited only by the space available.
</p><p>    Purpose: The purpose of the workshop is to summarize the body of 
scientific evidence, describe the gaps in knowledge, provide direction 
for future research, and offer guidance for appropriate public health  action if warranted.</p><p>    Matters To Be Discussed: The agenda will include an overview of the 
prevalence of thyroid dysfunction in reproductiveage women and factors 
associated with abnormal function, outcomes related to thyroid 
dysfunction during pregnancy, detection and treatment of thyroid 
dysfunction, and considerations for public health practice.
</p><p>    Agenda ite<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2003-12-05-03-30216</guid>
  <pubDate>Fri, Dec 5 2003 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Medicare Program; Coverage and Payment of Ambulance Services;  Inflation Update for CY 2004]]></title>
  <link>http://thefederalregister.com/d.p/2003-12-05-03-30152</link>
  <description><![CDATA[ This final rule provides the sunset date for the interim bonus 
payment for rural ambulance mileage of 18 through 50 miles as required 
by the Medicare, Medicaid and State Child Health Insurance Program 
Benefits Improvement and Protection Act of 2000 (BIPA) and provides 
notice of the annual Ambulance Inflation Factor (AIF) for ambulance 
services for calendar year (CY) 2004. The statute requires that this  inflation factor be<br/> [[Page 67961]]<br/>
applied in determining the fee schedule amounts and payment limits for 
ambulance services.
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  <guid>http://thefederalregister.com/d.p/2003-12-05-03-30152</guid>
  <pubDate>Fri, Dec 5 2003 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Medicare Program; Photocopying Reimbursement Methodology ]]></title>
  <link>http://thefederalregister.com/d.p/2003-12-05-03-30096</link>
  <description><![CDATA[ This final rule increases the rate of reimbursement for 
expenses incurred by prospective payment system (PPS) hospitals for 
photocopying medical records requested by Quality Improvement 
Organizations (QIOs), formerly known as Utilization and Quality Control 
Peer Review Organizations (PROs). We are increasing the rate from 7 
cents per page to 12 cents per page to reflect inflationary changes in  the labor and supply cost components of the formula.</p><p>    This final rule also provides for the periodic review and 
adjustment of the perpage reimbursement rate to account for inflation 
and changes in technology. The methodology for calculating the perpage  reimbursement rate will remain unchanged.</p><p>    We are also providing for the payment of the expenses of furnishing 
photocopies to QIOs, to other providers subject to a PPS (for example, 
skilled nursing facilities and home health agencies), in accordance 
with the rules established for reimbursing PPS hospitals for these 
expenses.
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  <guid>http://thefederalregister.com/d.p/2003-12-05-03-30096</guid>
  <pubDate>Fri, Dec 5 2003 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Agency Information Collection Activities: Proposed Collection;  Comment Request]]></title>
  <link>http://thefederalregister.com/d.p/2003-12-05-03-30200</link>
  <description><![CDATA[
</p><p>    Agency: Centers for Medicare and Medicaid Services, HHS.
</p><p>    In compliance with the requirement of section 3506(c)(2)(A) of the 
Paperwork Reduction Act of 1995, the Centers for Medicare and Medicaid 
Services (CMS) (formerly known as the Health Care Financing 
Administration (HCFA)), Department of Health and Human Services, is 
publishing the following summary of proposed collections for public 
comment. Interested persons are invited to send comments regarding this 
burden estimate or any other aspect of this collection of information, 
including any of the following subjects: (1) The necessity and utility 
of the proposed information collection for the proper performance of 
the agency's functions; (2) the accuracy of the estimated burden; (3) 
ways to enhance the quality, utility, and clarity of the information to 
be collected; and (4) the use of automated collection techniques or 
other forms of information technology to minimize the information  collection burden.</p><p>    1. Type of Information Collec<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2003-12-05-03-30200</guid>
  <pubDate>Fri, Dec 5 2003 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  National Heart, Lung, and Blood Institute (NHLBI): Opportunity  for Cooperative Research and Development Agreements]]></title>
  <link>http://thefederalregister.com/d.p/2003-12-05-03-30206</link>
  <description><![CDATA[ The National Heart, Lung, and Blood Institute (NHLBI) of the 
National Institutes of Health (NIH) announces the opportunity for 
Cooperative Research and Development Agreements (CRADAs) to develop 
novel mechanical and biological treatments in interventional 
cardiovascular medicine using xray fluoroscopy and realtime magnetic 
resonance imaging. The NHLBI seeks potential Collaborators wishing to 
provide expertise in (1) novel biological treatments for cardiovascular 
disease, including agents to facilitate mobilization of bonemarrow
derived stem and progenitor cells, (2) novel agents for therapeutic 
angiogenesis for myocardial or peripheral artery applications, (3) 
novel immunemodulating agents to treat to prevent manifestations of 
atherosclerosis, coronary artery occlusion, or myocardial ischemia/
infarction, (4) novel mechanisms of drug, gene, or cell delivery to the 
myocardium or skeletal muscle to treat manifestations of coronary or 
peripheral artery atherosclerosis, and (5) intravascular devices <script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2003-12-05-03-30206</guid>
  <pubDate>Fri, Dec 5 2003 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Government-Owned Inventions; Availability for Licensing ]]></title>
  <link>http://thefederalregister.com/d.p/2003-12-05-03-30207</link>
  <description><![CDATA[ The inventions listed below are owned by an agency of the U.S. 
Government and are available for licensing in the U.S. in accordance 
with 35 U.S.C. 207 to achieve expeditious commercialization of results 
of federallyfunded research and development. Foreign patent 
applications are filed on selected inventions to extend market coverage 
for companies and may also be available for licensing.
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  <guid>http://thefederalregister.com/d.p/2003-12-05-03-30207</guid>
  <pubDate>Fri, Dec 5 2003 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  National Institute of Child Health and Human Development; Notice  of Meeting]]></title>
  <link>http://thefederalregister.com/d.p/2003-12-05-03-30205</link>
  <description><![CDATA[
</p><p>    Pursuant to section 10(a) of the Federal Advisory Committee Act, as 
amended (5 U.S.C. Appendix 2), notice is hereby given of a meeting of 
the National Advisory Board on Medical Rehabilitation Research.
</p><p>    The meeting will be open to the public with attendance limited to 
space available. Individuals who plan to attend and need special 
assistance, such as sign language interpretation or other reasonable 
accommodations, should notify the Contact Person listed below in  advance of the meeting.</p><p>    Name of Committee: National Advisory Board on Medical  Rehabilitation Research.<br/> </p><p>    Date: December 89, 2003.<br/> </p><p>    Time: December 8, 2003, 8:30 a.m. to 5 p.m.</p><p>    Agenda: NICHD Director's Report presentation, Regional Research 
Networks, and an update on the Rehabilitation Medicine Scientist  Training Program.</p><p>    Place: Holiday InnSilver Spring, 8777 Georgia Avenue, Silver  Spring, MD 20910.<br/> </p><p>    Time: December 9, 2003, 8:30 a.m. to 12 p.m.</p><p>    Agenda: Other business dealing with the NABMRR Board.
</p><p>    Place: Ho<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2003-12-05-03-30205</guid>
  <pubDate>Fri, Dec 5 2003 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  National Institute of Diabetes and Digestive and Kidney Disease;  Amended Notice of Meeting]]></title>
  <link>http://thefederalregister.com/d.p/2003-12-05-03-30202</link>
  <description><![CDATA[
</p><p>    Notice is hereby given of a change in the meeting of the National 
Institute of Diabetes and Digestive and Kidney Diseases Special 
Emphasis Panel, November 25, 2003, 9 a.m. to November 25, 2003, 11 a.m. 
National Institutes of Health, Two Democracy Plaza, 6707 Democracy 
Boulevard, Bethesda, MD, 20892 which was published in the Federal  Register on October 31, 2003, 68 FR 62902.</p><p>    The meeting will be held on December 18, 2003 from 3 p.m. until 5  p.m. The meeting is closed to the public.<br/> </p><p>    Dated: November 28, 2003.<br/> Anna Snouffer,<br/>
Acting Director, Office of Federal Advisory Committee Policy. [FR Doc. 0330202 Filed 12403; 8:45 am]<br/>
BILLING CODE 414001M
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  <guid>http://thefederalregister.com/d.p/2003-12-05-03-30202</guid>
  <pubDate>Fri, Dec 5 2003 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/2003-12-05-03-30203</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 property.
</p><p>    Name of Committee: National Institute of Diabetes and Digestive 
Kidney Diseases Special Emphasis Panel, Chronic Kidney Disease. </p><p>    Date: December 12, 2003.<br/> </p><p>    Time: 3 p.m. to 4:30 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, (Telephone Conference  Call).<br/>
 <script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2003-12-05-03-30203</guid>
  <pubDate>Fri, Dec 5 2003 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/2003-12-05-03-30204</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.<br/> </p><p>    Date: December 10, 2003.<br/> </p><p>    Time: 10:30 a.m. to 1:30 p.m.</p><p>    Agenda: To review and evaluate grant applications.
</p><p>    Place: National Institutes of Health, Neuroscience Center, 6001 
Executive Boulevard, Rockville, MD 20852, (Telephone Conference  Call).</p><p>    Contact Person: David I. Sommers, PhD, Sci<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2003-12-05-03-30204</guid>
  <pubDate>Fri, Dec 5 2003 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Center for Scientific Review; Amended Notice of Meeting ]]></title>
  <link>http://thefederalregister.com/d.p/2003-12-05-03-30201</link>
  <description><![CDATA[
</p><p>    Notice is hereby given of a change in the meeting of the Center for 
Scientific Review Special Emphasis Panel, December 18, 2003, 1 p.m. to 
December 18, 2003, 3 p.m., National Institutes of Health, 6701 
Rockledge Drive, Bethesda, MD 20892 which was published in the Federal  Register on November 26, 2003, 68 FR 6647166472.</p><p>    The meeting will be held on December 19, 2003, from 5 p.m. to 7 
p.m. The location remains the same. The meeting is closed to the  public.<br/> </p><p>    Dated: November 28, 2003.<br/> Anna Snouffer,<br/>
Acting Director, Office of Federal Advisory Committee Policy. [FR Doc. 0330201 Filed 12403; 8:45 am]<br/>
BILLING CODE 414001M
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  <guid>http://thefederalregister.com/d.p/2003-12-05-03-30201</guid>
  <pubDate>Fri, Dec 5 2003 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Current List of Laboratories Which Meet Minimum Standards To  Engage in Urine Drug Testing for Federal Agencies]]></title>
  <link>http://thefederalregister.com/d.p/2003-12-05-03-30217</link>
  <description><![CDATA[ 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) published in the 
Federal Register on April 11, 1988 (53 FR 11970), and revised in the 
Federal Register on June 9, 1994 (59 FR 29908) and on September 30, 
1997 (62 FR 51118). 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.</p><p>    If any laboratory has withdrawn from 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.
</p><p>    This notice is also available on the Internet at <A H<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2003-12-05-03-30217</guid>
  <pubDate>Fri, Dec 5 2003 11:00:00 GMT</pubDate>
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