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    <title>The Federal Register</title>
    <link>http://thefederalregister.com/b.p/department/DEPARTMENT_OF_HEALTH_AND_HUMAN_SERVICES/2007-12-12/</link>
    <description>Daily Publications of Meetings and Rules Changes for the Federal Government</description>
    <pubDate>Fri, Sep 5 2008 11:00:00 GMT</pubDate>
    <lastBuildDate>Fri, Sep 5 2008 11:00:00 GMT</lastBuildDate>
    <webMaster>info@thefederalregister.com</webMaster>
    <item>
  <title><![CDATA[  Notice of Public Meeting and Availability for Public Comment]]></title>
  <link>http://thefederalregister.com/d.p/2007-12-12-E7-24047</link>
  <description><![CDATA[ The National Institute for Occupational Safety and Health 
(NIOSH) of the Centers for Disease Control and Prevention (CDC) 
announces the following meeting and request for public comment on the 
draft Current Intelligence Bulletin (CIB) entitled ``Interim Guidance 
on Medical Screening of Workers Potentially Exposed to Engineered 
Nanoparticles.'' The document and instructions for submitting comments 
can be found at <A HREF="/i.p/outbound/http://www.cdc.gov/niosh/review/public/115/">http://www.cdc.gov/niosh/review/public/115/</A>. Comments 
may be provided to the NIOSH docket, as well as given orally at the  following meeting.</p><p>    Public Comment Period: December 14, 2007 through February 15, 2008.
</p><p>    Public Meeting Time and Date: 9 a.m.4 p.m., January 30, 2008.
</p><p>    Place: Robert A. Taft Laboratories, Taft Auditorium, NIOSH, CDC,  4676 Columbia Parkway, Cincinnati, Ohio 45226.</p><p>    Purpose of Meeting: To discuss and obtain comments on th<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2007-12-12-E7-24047</guid>
  <pubDate>Wed, Dec 12 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Agency Emergency Processing Under the Office of Management and  Budget Review; Certification to Accompany Drug,]]></title>
  <link>http://thefederalregister.com/d.p/2007-12-12-07-6023</link>
  <description><![CDATA[ The Food and Drug Administration (FDA) is announcing that a 
proposed collection of information has been submitted to the Office of 
Management and Budget (OMB) for emergency processing under the 
Paperwork Reduction Act of 1995 (the PRA). The proposed collection of 
information concerns the certification to accompany human drug, 
biological product, and device applications or submissions.
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  <guid>http://thefederalregister.com/d.p/2007-12-12-07-6023</guid>
  <pubDate>Wed, Dec 12 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[
Agency Information Collection Request. 60-Day Public Comment  Request]]></title>
  <link>http://thefederalregister.com/d.p/2007-12-12-E7-24054</link>
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  <guid>http://thefederalregister.com/d.p/2007-12-12-E7-24054</guid>
  <pubDate>Wed, Dec 12 2007 11:00:00 GMT</pubDate>
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<item>
  <title><![CDATA[
Agency Information Collection Request. 60-Day Public Comment  Request]]></title>
  <link>http://thefederalregister.com/d.p/2007-12-12-E7-24055</link>
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  <guid>http://thefederalregister.com/d.p/2007-12-12-E7-24055</guid>
  <pubDate>Wed, Dec 12 2007 11:00:00 GMT</pubDate>
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<item>
  <title><![CDATA[  Agency Information Collection Activities: Submission for OMB  Review; Comment Request]]></title>
  <link>http://thefederalregister.com/d.p/2007-12-12-E7-24022</link>
  <description><![CDATA[
</p><p>    Periodically, the Health Resources and Services Administration 
(HRSA) publishes abstracts of information collection requests under 
review by the Office of Management and Budget (OMB), in compliance with 
the Paperwork Reduction Act of 1995 (44 U.S.C. Chapter 35). To request 
a copy of the clearance requests submitted to OMB for review, call the  HRSA Reports Clearance Office on (301) 4431129.</p><p>    The following request has been submitted to OMB for review under  the Paperwork Reduction Act of 1995:<br/>
Proposed Project: Ryan White HIV/AIDS Program Annual Data Report: Data  Report Form: (OMB No. 09150253)Revision</p><p>    The Ryan White HIV/AIDS Program Annual Data Report, formerly called 
the CARE Act Data Report (CADR), was first implemented in 2002 by 
HRSA's HIV/AIDS Bureau. It has undergone revisions to incorporate the 
legislative changes that occurred in 2006. Grantees and their 
subcontracted service providers who are funded under Parts A, B, C, and 
D of Title XXVI of the Public Health Service Act, as am<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2007-12-12-E7-24022</guid>
  <pubDate>Wed, Dec 12 2007 11:00:00 GMT</pubDate>
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