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    <title>The Federal Register</title>
    <link>http://thefederalregister.com/b.p/department/DEPARTMENT_OF_HEALTH_AND_HUMAN_SERVICES/2005-12-23/</link>
    <description>Daily Publications of Meetings and Rules Changes for the Federal Government</description>
    <pubDate>Sat, Nov 22 2008 11:00:00 GMT</pubDate>
    <lastBuildDate>Sat, Nov 22 2008 11:00:00 GMT</lastBuildDate>
    <webMaster>info@thefederalregister.com</webMaster>
    <item>
  <title><![CDATA[  Medicare Program; E-Prescribing and the Prescription Drug  Program; Correction]]></title>
  <link>http://thefederalregister.com/d.p/2005-12-23-05-24445</link>
  <description><![CDATA[ This document corrects technical errors that appeared in the 
final rule published in the Federal Register on November 7, 2005, 
entitled ``Medicare Program; EPrescribing and the Prescription Drug 
Program.''
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  <guid>http://thefederalregister.com/d.p/2005-12-23-05-24445</guid>
  <pubDate>Fri, Dec 23 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Medicare and Medicaid Programs: Reporting Outcome and Assessment  Information Set Data as Part of the Conditions of]]></title>
  <link>http://thefederalregister.com/d.p/2005-12-23-05-24389</link>
  <description><![CDATA[ This final rule makes revisions in response to public comments 
received on the January 25, 1999 interim final rule with comment period 
(64 FR 3748). The interim final rule requires electronic reporting of 
data from the Outcome and Assessment Information Set as a Condition of 
Participation for home health agencies.
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  <guid>http://thefederalregister.com/d.p/2005-12-23-05-24389</guid>
  <pubDate>Fri, Dec 23 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Medicare Program; Hospice Wage Index for Fiscal Year 2006 ]]></title>
  <link>http://thefederalregister.com/d.p/2005-12-23-05-24288</link>
  <description><![CDATA[ This document corrects technical errors that appeared in the 
final rule published in the Federal Register on August 4, 2005, 
entitled ``Hospice Wage Index for Fiscal Year 2006.''
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  <guid>http://thefederalregister.com/d.p/2005-12-23-05-24288</guid>
  <pubDate>Fri, Dec 23 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Medicare Program; Changes to the Hospital Outpatient Prospective  Payment System and Calendar Year 2006 Payment Rates;]]></title>
  <link>http://thefederalregister.com/d.p/2005-12-23-05-24447</link>
  <description><![CDATA[ This document corrects technical errors that appeared in the 
final rule with comment period published in the Federal Register on 
November 10, 2005 entitled ``Changes to the Hospital Outpatient 
Prospective Payment System and Calendar Year 2006 Payment Rates; Final 
Rule.''
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  <guid>http://thefederalregister.com/d.p/2005-12-23-05-24447</guid>
  <pubDate>Fri, Dec 23 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  New Animal Drugs; Moxidectin ]]></title>
  <link>http://thefederalregister.com/d.p/2005-12-23-05-24386</link>
  <description><![CDATA[ The Food and Drug Administration (FDA) is amending the animal 
drug regulations to reflect approval of a new animal drug application 
(NADA) filed by Fort Dodge Animal Health, Division of Wyeth. The NADA 
provides for oral use of moxidectin solution in sheep for the treatment 
and control of a variety of internal parasites.
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  <guid>http://thefederalregister.com/d.p/2005-12-23-05-24386</guid>
  <pubDate>Fri, Dec 23 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Medicare Program; Establishment of the Medicare Advantage Program]]></title>
  <link>http://thefederalregister.com/d.p/2005-12-23-05-24446</link>
  <description><![CDATA[ This document corrects technical errors that appeared in the 
final rule published in the Federal Register on January 28, 2005 
entitled ``Establishment of the Medicare Advantage Program.''
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  <guid>http://thefederalregister.com/d.p/2005-12-23-05-24446</guid>
  <pubDate>Fri, Dec 23 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Food Labeling: Health Claims; Soluble Dietary Fiber From Certain  Foods and Coronary Heart Disease]]></title>
  <link>http://thefederalregister.com/d.p/2005-12-23-05-24387</link>
  <description><![CDATA[ The Food and Drug Administration (FDA) is amending the 
regulation authorizing a health claim on the relationship between oat 
betaglucan soluble fiber and reduced risk of coronary heart disease 
(CHD). The amendment adds barley as an additional eligible source of 
betaglucan soluble fiber. We (FDA) are taking this action in response 
to a petition that the National Barley Foods Council submitted. We have 
concluded, based on the totality of publicly available scientific 
evidence that, in addition to certain oat products, whole grain barley 
and certain dry milled barley grain products are appropriate sources of 
betaglucan soluble fiber for the health claim.
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  <guid>http://thefederalregister.com/d.p/2005-12-23-05-24387</guid>
  <pubDate>Fri, Dec 23 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Agency Information Collection Activities: Proposed Collection;  Comment Request]]></title>
  <link>http://thefederalregister.com/d.p/2005-12-23-05-24301</link>
  <description><![CDATA[<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2005-12-23-05-24301</guid>
  <pubDate>Fri, Dec 23 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Agency Information Collection Activities; Proposed Collection;  Comment Request; Medical Device Reporting:]]></title>
  <link>http://thefederalregister.com/d.p/2005-12-23-E5-7726</link>
  <description><![CDATA[ The Food and Drug Administration (FDA) is announcing an 
opportunity for public comment on the proposed collection of certain 
information by the agency. Under the Paperwork Reduction Act of 1995 
(the PRA), Federal agencies are required to publish notice in the 
Federal Register concerning each proposed collection of information, 
including each proposed extension of an existing collection of 
information, and to allow 60 days for public comment in response to the 
notice. This notice solicits comments on Medical Device Reporting: 
Manufacturer Reporting, Importer Reporting, User Facility Reporting, 
and Distributor Reporting.
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  <guid>http://thefederalregister.com/d.p/2005-12-23-E5-7726</guid>
  <pubDate>Fri, Dec 23 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Agency Information Collection Activities: Submission for OMB  Review; Comment Request]]></title>
  <link>http://thefederalregister.com/d.p/2005-12-23-05-24302</link>
  <description><![CDATA[<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2005-12-23-05-24302</guid>
  <pubDate>Fri, Dec 23 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Medicare and Medicaid Programs; Quarterly Listing of Program  Issuances--July Through September 2005]]></title>
  <link>http://thefederalregister.com/d.p/2005-12-23-05-24023</link>
  <description><![CDATA[ This notice lists CMS manual instructions, substantive and 
interpretive regulations, and other Federal Register notices that were 
published from July 2005 through September 2005, relating to the 
Medicare and Medicaid programs. This notice provides information on 
national coverage determinations (NCDs) affecting specific medical and 
health care services under Medicare. Additionally, this notice 
identifies certain devices with investigational device exemption (IDE) 
numbers approved by the Food and Drug Administration (FDA) that 
potentially may be covered under Medicare. This notice also includes 
listings of all approval numbers from the Office of Management and 
Budget for collections of information in CMS regulations. Finally, this 
notice includes a list of Medicareapproved carotid stent facilities.
</p><p>    Section 1871(c) of the Social Security Act requires that we publish 
a list of Medicare issuances in the Federal Register at least every 3 
months. Although we are not mandated to do so by statute, f<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2005-12-23-05-24023</guid>
  <pubDate>Fri, Dec 23 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Medicare Program: Meeting of the Advisory Panel on Ambulatory  Payment Classification (APC) Groups--March 1, 2, and 3,]]></title>
  <link>http://thefederalregister.com/d.p/2005-12-23-05-24290</link>
  <description><![CDATA[ In accordance with section 10(a) of the Federal Advisory 
Committee Act (FACA) (5 U.S.C. Appendix 2), this notice announces the 
first biannual meeting of the Ambulatory Payment Classification (APC)  Panel (the Panel) for 2006.</p><p>    The purpose of the Panel is to review the APC groups and their 
associated weights and to advise the Secretary of the Department of 
Health and Human Services (HHS) and the Administrator of the Centers 
for Medicare & Medicaid Services (CMS) concerning the clinical 
integrity of the APC groups and their associated weights. The advice 
provided by the Panel will be considered as CMS prepares its annual 
updates of the hospital Outpatient Prospective Payment System (OPPS) 
through rulemaking.
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  <guid>http://thefederalregister.com/d.p/2005-12-23-05-24290</guid>
  <pubDate>Fri, Dec 23 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Medicare Program; Town Hall Meeting on the Fiscal Year 2007  Applications for New Medical Services and Technologies]]></title>
  <link>http://thefederalregister.com/d.p/2005-12-23-05-24022</link>
  <description><![CDATA[ This notice, in accordance with section 1886(d)(5)(K)(viii) of 
the Social Security Act (the Act), announces a Town Hall meeting to 
discuss fiscal year (FY) 2007 applications for addon payments for new 
medical services and technologies under the hospital inpatient 
prospective payment system (IPPS). Interested parties are invited to 
this meeting to present their individual comments, recommendations, and 
data regarding whether the FY 2007 new medical services and 
technologies applications meet the substantial clinical improvement 
criteria.
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  <guid>http://thefederalregister.com/d.p/2005-12-23-05-24022</guid>
  <pubDate>Fri, Dec 23 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Consolidated Health Informatics (CHI) Initiative; Health Care and  Vocabulary Standards for Use in Federal Health]]></title>
  <link>http://thefederalregister.com/d.p/2005-12-23-05-24289</link>
  <description><![CDATA[ This notice identifies the 20 messaging and vocabulary 
standards adopted for use in Federal government health information 
technology systems. The first set of 5 standards was adopted on March 
21, 2003. The second set of 15 standards was adopted on May 6, 2004,  thus completing the initial portfolio of<br/> [[Page 76288]]<br/>
the Consolidated Health Informatics (CHI) initiative.
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  <guid>http://thefederalregister.com/d.p/2005-12-23-05-24289</guid>
  <pubDate>Fri, Dec 23 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Medicare Program; Meeting of the Advisory Panel on Medicare  Education, January 26, 2006]]></title>
  <link>http://thefederalregister.com/d.p/2005-12-23-E5-7757</link>
  <description><![CDATA[ In accordance with the Federal Advisory Committee Act, 5 
U.S.C. Appendix 2, section 10(a) (Pub. L. 92463), this notice 
announces a meeting of the Advisory Panel on Medicare Education (the 
Panel) on January 26, 2006. The Panel advises and makes recommendations 
to the Secretary of Health and Human Services and the Administrator of 
the Centers for Medicare & Medicaid Services on opportunities to 
enhance the effectiveness of consumer education strategies concerning 
the Medicare program. This meeting is open to the public.
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  <guid>http://thefederalregister.com/d.p/2005-12-23-E5-7757</guid>
  <pubDate>Fri, Dec 23 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Simplification of the Grant Appeals Process ]]></title>
  <link>http://thefederalregister.com/d.p/2005-12-23-05-24442</link>
  <description><![CDATA[ The Department of Health and Human Services (HHS) is amending 
regulations to remove the Health Resources and Services Administration 
(HRSA) from the list of agencies which require grantees to utilize an 
informal appeals procedure for grant related disputes subject to the 
departmental appeal procedures. In doing so, HRSA will simplify the 
appeals procedure for aggrieved HRSA grantees by permitting them direct 
access to the Departmental Grant Appeals Board.
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  <pubDate>Fri, Dec 23 2005 11:00:00 GMT</pubDate>
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