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    <title>The Federal Register</title>
    <link>http://thefederalregister.com/b.p/agency/National_Institutes_of_Health/2006-12-12/</link>
    <description>Daily Publications of Meetings and Rules Changes for the Federal Government</description>
    <pubDate>Tue, Dec 2 2008 11:00:00 GMT</pubDate>
    <lastBuildDate>Tue, Dec 2 2008 11:00:00 GMT</lastBuildDate>
    <webMaster>info@thefederalregister.com</webMaster>
    <item>
  <title><![CDATA[  Government-Owned Inventions; Availability for Licensing ]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-12-E6-21028</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.<br/>
[[Page 74547]]
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  <guid>http://thefederalregister.com/d.p/2006-12-12-E6-21028</guid>
  <pubDate>Tue, Dec 12 2006 11:00:00 GMT</pubDate>
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<item>
  <title><![CDATA[  Government-Owned Inventions; Availability for Licensing ]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-12-E6-21029</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/2006-12-12-E6-21029</guid>
  <pubDate>Tue, Dec 12 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Government-Owned Inventions; Availability for Licensing ]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-12-E6-21037</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/2006-12-12-E6-21037</guid>
  <pubDate>Tue, Dec 12 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  National Library of Medicine; Notice of Meeting ]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-12-06-9631</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 open to the public as indicated below, 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>    The portions of the meeting devoted to the review and evaluation of 
journals for potential indexing by the National Library of Medicine 
will be closed to the public in accordance with the provisions set 
forth in section 552b(c)(9)(B), Title 5 U.S.C., as amended. Premature 
disclosure of the titles of the journals as potential titles to be 
indexed by the National Library of Medicine, the discussions, and the 
presence of individuals associated with these publications could 
significantly frustrate the review and evaluation of individual 
j<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2006-12-12-06-9631</guid>
  <pubDate>Tue, Dec 12 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[
National Toxicology Program (NTP); Center for the Evaluation of  Risks to Human Reproduction (CERHR); Availability of]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-12-E6-21040</link>
  <description><![CDATA[ The CERHR announces the availability of the draft expert panel 
report for bisphenol A on December 15, 2006, from the CERHR Web site 
(<A HREF="/i.p/outbound/http://cerhr.niehs.nih.gov">http://cerhr.niehs.nih.gov</A>) or in printed text from CERHR (see FOR 
FURTHER INFORMATION CONTACT below). The CERHR invites the submission of 
public comments on sections 14 of the draft expert panel report (see 
SUPPLEMENTARY INFORMATION below). The expert panel will meet on March 
57, 2007, at the Radisson Hotel Old Town in Alexandria, Virginia to 
review and revise the draft expert panel report and reach conclusions 
regarding whether exposure to bisphenol A is a hazard to human 
development or reproduction. The expert panel will also identify data 
gaps and research needs. CERHR expert panel meetings are open to the 
public with time scheduled for oral public comment. Attendance is 
limited only by the available meeting room space. Following the exp<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2006-12-12-E6-21040</guid>
  <pubDate>Tue, Dec 12 2006 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/2006-12-12-E6-21038</link>
  <description><![CDATA[ NICEATM in collaboration with the Interagency Coordinating 
Committee on the Validation of Alternative Methods (ICCVAM) announces 
an independent scientific peer review meeting to evaluate the 
validation status of five in vitro pyrogenicity test methods: (1) Human 
PBMC/IL6 in vitro pyrogen test (PBMC/IL6), (2) human whole blood/IL1 
in vitro pyrogen test (WB/IL1), (3) human whole blood/IL1 in vitro 
pyrogen test: application of cryopreserved human whole blood (cryo WB/
IL1), (4) the human whole blood/IL6 in vitro pyrogen test (WB/IL6), 
and (5) an alternative in vitro pyrogen test using the human monocytoid 
cell line MONO MAC6 (MM6/IL6). These five in vitro test methods are 
proposed as replacements for the in vivo rabbit pyrogen test (RPT). At 
this meeting, a scientific panel will peer review the draft background 
review document (BRD) on each test method, evaluate the extent that the 
BRD addresses established validation and acceptance criteria for each 
test method, and provide comment on draft ICCVAM<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2006-12-12-E6-21038</guid>
  <pubDate>Tue, Dec 12 2006 11:00:00 GMT</pubDate>
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