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    <title>The Federal Register</title>
    <link>http://thefederalregister.com/b.p/department/DEPARTMENT_OF_HEALTH_AND_HUMAN_SERVICES/2006-12-08/</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[  Agency Information Collection Activities; Proposed Collection;  Comment Request; Alzheimer's Disease Demonstration]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-E6-20890</link>
  <description><![CDATA[ The Administration on Aging (AoA) 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 the information collection requirements relating 
to Alzheimer's Disease Demonstration Grants to States Program
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  <guid>http://thefederalregister.com/d.p/2006-12-08-E6-20890</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Agency Forms Undergoing Paperwork Reduction Act Review ]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-E6-20855</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>    Application for TrainingRevisionOffice of Workforce and Career 
Development (OWCD), Centers for Disease Control and Prevention (CDC). Background and Brief Description</p><p>    The Centers for Disease Control and Prevention (CDC) through its 
Office of Workforce and Career Development (OWCD) and other Centers, 
Institutes, and Offices offers training activities on public health 
topics to professionals worldwide. E<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2006-12-08-E6-20855</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  CDC/HRSA Advisory Committee on HIV and STD Prevention and  Treatment: Notice of Charter Renewal]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-E6-20853</link>
  <description><![CDATA[
</p><p>    This gives notice under the Federal Advisory Committee Act (Pub. L. 
92463) of October 6, 1972, that the CDC/HRSA Advisory Committee on HIV 
and STD Prevention and Treatment Centers for Disease Control and 
Prevention, Department of Health and Human Services, has been renewed  for a 2year period through November 25, 2008.</p><p>    For information, contact Kevin Fenton, M.D., Ph.D., Executive 
Secretary, CDC/HRSA Advisory Committee on HIV and STD Prevention and 
Treatment, Centers for Disease Control and Prevention, Department of 
Health and Human Services, 1600 Clifton Road, NE., Mailstop E07, 
Atlanta, Georgia 30333, telephone 404/6398000 or fax 404/6398600.
</p><p>    The Director, Management Analysis and Services Office, has been 
delegated the authority to sign Federal Register notices pertaining to 
announcements of meetings and other committee management activities, 
for both the Centers for Disease Control and Prevention and the Agency  for Toxic Substances and Disease Registry.<br/> </p><p>    Dated: December 1, 2006.<br/>
A<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2006-12-08-E6-20853</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Decision To Evaluate a Petition to Designate a Class of Employees  at Hanford Nuclear Reservation, Richland, WA, To Be]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-06-9585</link>
  <description><![CDATA[ The Department of Health and Human Services (HHS) gives notice 
as required by 42 CFR Sec.  83.12(e) of a decision to evaluate a 
petition to designate a class of employees at the Hanford Nuclear 
Reservation, Richland, Washington, to be included in the Special 
Exposure Cohort under the Energy Employees Occupational Illness 
Compensation Program Act of 2000. The initial proposed definition for 
the class being evaluated, subject to revision as warranted by the  evaluation, is as follows:<br/> </p><p>    Facility: Hanford Nuclear Reservation.<br/> </p><p>    Location: Richland, Washington.<br/> </p><p>    Job Titles and/or Job Duties: All employees.</p><p>    Period of Employment: January 2, 1942 through December 31, 1990.
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  <guid>http://thefederalregister.com/d.p/2006-12-08-06-9585</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Designation of a Class of Employees for Addition to the Special  Exposure Cohort]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-06-9587</link>
  <description><![CDATA[ The Department of Health and Human Services (HHS) gives notice 
of a decision to designate a class of employees at the Los Alamos 
National Laboratory, Los Alamos, New Mexico, as an addition to the 
Special Exposure Cohort (SEC) under the Energy Employees Occupational 
Illness Compensation Program Act of 2000. On November 9, 2006, the 
Secretary of HHS designated the following class of employees as an  addition to the SEC:</p><p>    Employees of the Department of Energy predecessor agencies and  their contractors or<br/> [[Page 71175]]<br/>
subcontractors who were monitored or should have been monitored for 
exposure to ionizing radiation associated with radioactive lanthanum 
(RaLa) operations at Technical Area 10 (Bayo Canyon Site), Technical 
Area 35 (Ten Site), and Buildings H, Sigma, and U (located within 
Technical Area 1) for a number of work days aggregating at least 250 
work days during the period from September 1, 1944, through July 18, 
1963, or in combination with work days within the parameters 
established fo<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2006-12-08-06-9587</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Designation of a Class of Employees for Addition to the Special  Exposure Cohort]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-06-9586</link>
  <description><![CDATA[ The Department of Health and Human Services (HHS) gives notice 
of a decision to designate a class of employees at the Oak Ridge 
Institute of Nuclear Studies Cancer Research Hospital, Oak Ridge, 
Tennessee, as an addition to the Special Exposure Cohort (SEC) under 
the Energy Employees Occupational Illness Compensation Program Act of 
2000. On November 9, 2006, the Secretary of HHS designated the  following class of employees as an addition to the SEC:</p><p>    Employees of the Department of Energy (DOE) predecessor agencies 
and their contractors or subcontractors who were monitored or should 
have been monitored while working at the Oak Ridge Institute of 
Nuclear Studies Cancer Research Hospital from May 15, 1950, through 
December 31, 1963, and who were employed for a number of work days 
aggregating at least 250 work days or in combination with work days 
within the parameters established for other classes of employees  included in the SEC.</p><p>    This designation will become effective on December 9, 2006, unl<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2006-12-08-06-9586</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Designation of a Class of Employees for Addition to the Special  Exposure Cohort]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-06-9588</link>
  <description><![CDATA[ The Department of Health and Human Services (HHS) gives notice 
of a decision to designate a class of employees at the Oak Ridge 
Thermal Diffusion Plant (S50), Oak Ridge, Tennessee, as an addition to 
the Special Exposure Cohort (SEC) under the Energy Employees 
Occupational Illness Compensation Program Act of 2000. On November 9, 
2006, the Secretary of HHS designated the following class of employees  as an addition to the SEC:</p><p>    Employees of the Department of Energy predecessor agencies and 
their contractors and subcontractors who were monitored or should 
have been monitored while working at the S50 Oak Ridge Thermal 
Diffusion Plant working for a number of work days aggregating at 
least 250 work day during the period from July 9, 1944, through 
December 31, 1951, or in combination with work days within the 
parameters established for one or more other classes of employees in  the SEC.</p><p>    This designation will become effective on December 9, 2006, unless 
Congress provides otherwise prior to the eff<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2006-12-08-06-9588</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Advisory Committee on Immunization Practices: Meeting ]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-E6-20859</link>
  <description><![CDATA[
</p><p>    In accordance with section 10(a)(2) of the Federal Advisory 
Committee Act (Pub. L. 92463), the Centers for Disease Control and 
Prevention (CDC) announces the following Federal Committee meeting.
</p><p>    Name: Advisory Committee on Immunization Practices (ACIP).
</p><p>    Times and Dates: 8 a.m.6 p.m., February 21, 2007, 8 a.m.4  p.m., February 22, 2007.</p><p>    Place: Centers for Disease Control and Prevention, 1600 Clifton 
Road, NE., Global Communications Center, Building 19, Room 232,  Atlanta, Georgia 30333.</p><p>    Status: Open to the public, limited only by the space available. 
Meeting space accommodates approximately 330 people. Overflow space  for realtime viewing will be available.</p><p>    Purpose: The Committee is charged with advising the Director, 
CDC, on the appropriate uses of immunizing agents. In addition, 
under 42 U.S.C. Sec.  1396s, the Committee is mandated to establish 
and periodically review and, as appropriate, revise the list of 
vaccines for administration to vaccineeligible children through the <script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2006-12-08-E6-20859</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[CMS-1321-CN RIN 0938-AN84 ]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-06-9550</link>
  <description><![CDATA[ This correction document corrects a limited number of 
technical and typographical errors in the final rule with comment 
period that appeared in the December 1, 2006 Federal Register (71 FR 
69624). The final rule with comment period addressed Medicare Part B 
payment policy, including the physician fee schedule (PFS) that is 
applicable for calendar year (CY) 2007, finalized the CY 2006 interim 
relative value units (RVUs), and established interim RVUs for new and 
revised procedure codes for CY 2007.
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  <guid>http://thefederalregister.com/d.p/2006-12-08-06-9550</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Medicare and Medicaid Programs; Hospital Conditions of  Participation: Patients' Rights]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-06-9559</link>
  <description><![CDATA[ This final rule finalizes the Patients' Rights Condition of 
Participation (CoP) which is applicable to all Medicare and Medicaid
participating hospitals and contains standards that ensure minimum 
protections of each patient's physical and emotional health and safety. 
It responds to comments on the following standards presented in the 
July 2, 1999 interim final rule: Notice of rights; exercise of rights; 
privacy and safety; confidentiality of patient records; restraint for 
acute medical and surgical care; and seclusion and restraints for 
behavior management. As a result of comments received, we have revised 
the standards regarding restraint and seclusion and set forth standards 
regarding staff training and death reporting.
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  <guid>http://thefederalregister.com/d.p/2006-12-08-06-9559</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Medicare and Medicaid Programs; Programs of All-Inclusive Care  for the Elderly (PACE); Program Revisions]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-E6-20544</link>
  <description><![CDATA[ This rule finalizes the interim final rule with comment period 
published in the Federal Register November 24, 1999 (64 FR 66234) and 
the interim final rule with comment period published in the Federal 
Register on October 1, 2002 (67 FR 61496). The November 1999 interim 
final rule implemented sections 4801 through 4803 of the Balanced 
Budget Act of 1997 (Pub. L. 10533) and established requirements for 
Programs of Allinclusive Care for the Elderly (PACE) under the 
Medicare and Medicaid programs. The interim final rule with comment 
period published on October 1, 2002 (67 FR 61496) implemented section 
903 of the Medicare, Medicaid, and SCHIP Benefits Improvement and 
Protection Act of 2000 (BIPA) (Pub. L. 106554).
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  <guid>http://thefederalregister.com/d.p/2006-12-08-E6-20544</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Emergency Clearance: Public Information Collection Requirements  Submitted to the Office of Management and Budget]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-E6-20543</link>
  <description><![CDATA[<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2006-12-08-E6-20543</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Emergency Clearance: Public Information Collection Requirements  Submitted to the Office of Management and Budget]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-E6-20665</link>
  <description><![CDATA[<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2006-12-08-E6-20665</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Emergency Clearance: Public Information Collection Requirements  Submitted to the Office of Management and Budget]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-E6-20666</link>
  <description><![CDATA[<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2006-12-08-E6-20666</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Agency Information Collection Activities: Proposed Collection;  Comment Request]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-E6-20678</link>
  <description><![CDATA[<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2006-12-08-E6-20678</guid>
  <pubDate>Fri, Dec 8 2006 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/2006-12-08-E6-20679</link>
  <description><![CDATA[<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2006-12-08-E6-20679</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Oral Dosage Form New Animal Drugs; Lincomycin and Spectinomycin  Powder]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-E6-20929</link>
  <description><![CDATA[  The Food and Drug Administration (FDA) is amending the animal 
drug regulations to reflect approval of an abbreviated new animal drug 
application (ANADA) filed by Agri Laboratories, Ltd. The ANADA provides 
for the oral use of lincomycin and spectinomycin soluble powder to 
create a solution administered in the drinking water of chickens as an 
aid in the control of airsacculitis.
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  <guid>http://thefederalregister.com/d.p/2006-12-08-E6-20929</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Oral Dosage Form New Animal Drugs; Oxytetracycline Powder ]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-E6-20928</link>
  <description><![CDATA[ The Food and Drug Administration (FDA) is amending the animal 
drug regulations to reflect approval of a supplemental abbreviated new 
animal drug application (ANADA) filed by IVX Animal Health, Inc. The 
supplemental ANADA revises labeling of generic oxytetracycline soluble 
powder with the current scientific names of the causative bacteria of 
foulbrood of honeybees.
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]]></description>
  <guid>http://thefederalregister.com/d.p/2006-12-08-E6-20928</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  30-Day Notice; Agency Information Collection Activities: Proposed  Collection; Comment Request]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-E6-20915</link>
  <description><![CDATA[<script type="text/javascript">
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]]></description>
  <guid>http://thefederalregister.com/d.p/2006-12-08-E6-20915</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  30-Day Notice; Agency Information Collection Activities: Proposed  Collection; Comment Request]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-E6-20916</link>
  <description><![CDATA[<script type="text/javascript">
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]]></description>
  <guid>http://thefederalregister.com/d.p/2006-12-08-E6-20916</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[
Draft Guidance on Engagement of Institutions in Human Subjects  Research]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-E6-20849</link>
  <description><![CDATA[ The Office for Human Research Protections (OHRP), Office of 
Public Health and Science, is announcing the availability of a draft 
guidance document entitled, ``OHRP Guidance on Engagement of 
Institutions in Human Subjects Research.'' The draft guidance document 
would revise and replace two existing OHRP guidance documents on the 
engagement of institutions in human subjects research: (1) The January 
26, 1999 document on ``Engagement of Institutions in Research, and (2) 
the December 23, 1999 document on ``Engagement of Pharmaceutical 
Companies in HHS Supported Research.'' To facilitate public review of 
the draft guidance document, OHRP has developed a table presenting a 
sidebyside comparison of OHRP's draft revised guidance document and 
the current guidance documents on the engagement of institution in 
human subjects research, which is available on the OHRP Web site at 
<A HREF="/i.p/outbound/http://www.hhs.gov/ohrp/requests/">h<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2006-12-08-E6-20849</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Findings of Research Misconduct ]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-E6-20927</link>
  <description><![CDATA[ Notice is hereby given that the Office of Research Integrity 
(ORI) and the Assistant Secretary for Health have taken final action in  the following case:</p><p>    Nicholas McMaster, University of Chicago: Based on a College 
Discipline Hearing report and on additional analysis conducted by ORI 
in its oversight review, the U.S. Public Health Service (PHS) found 
that Mr. Nicholas McMaster, undergraduate student, Biological Sciences 
Collegiate Division in the Departments of Psychology and Comparative 
Human Development at the University of Chicago (UC), engaged in 
research misconduct supported by National Institute of Environmental 
Health Sciences (NIEHS), National Institutes of Health (NIH), grant P50 
ES12382 and National Institute on Aging (NIA), NIH, grant P01 AG018911.
</p><p>    Specifically, PHS found that Mr. McMaster fabricated data in 
recording the score for the lordosis reflex and in recording the cell 
types present in vaginal epithelium from rats in two experimental  psychology protocols.</p><p>    Mr. McMast<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2006-12-08-E6-20927</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Privacy Act of 1974; Revisions to OIG's Privacy Act System of  Records--Criminal Investigative Files]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-08-E6-20848</link>
  <description><![CDATA[ The Office of Inspector General (OIG) is revising the existing 
system of records, entitled ``Criminal Investigative Files'' (0990
0003), by updating the ``Systems Location'' section of that document, 
and republishing the revised system of records in its entirety. This 
notice is in accordance with the Privacy Act requirement that agencies 
publish their amended systems of records in the Federal Register when 
there is a revision, change, or addition. This system of records, 
maintained by OIG, was last revised and updated on June 19, 2003 (68 FR 
36828).
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]]></description>
  <guid>http://thefederalregister.com/d.p/2006-12-08-E6-20848</guid>
  <pubDate>Fri, Dec 8 2006 11:00:00 GMT</pubDate>
</item>
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