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<classification authority="sudocs">GA 1.13:GAO-07-1022T</classification>
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 <subject>Beneficiaries</subject>
 <subject>Claims processing</subject>
 <subject>Eligibility determinations</subject>
 <subject>Health care programs</subject>
 <subject>Internal controls</subject>
 <subject>Medicaid</subject>
 <subject>Medicare</subject>
 <subject>Monitoring</subject>
 <subject>Pharmaceutical industry</subject>
 <subject>Prescription drugs</subject>
 <subject>Prospective payments</subject>
 <subject>Reimbursements</subject>
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<titleInfo>
 <title>Medicare Part D: CMS&apos;s Process and Policy for Enrolling New Dual-Eligible Beneficiaries</title>
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<abstract>Under the Medicare Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA), dual-eligible			 
beneficiaries--individuals with both Medicare and Medicaid	 
coverage--have their drug costs covered under Medicare Part D	 
rather than under state Medicaid programs. The MMA requires the  
Centers for Medicare &amp; Medicaid Services (CMS) to enroll these	 
beneficiaries in a Medicare prescription drug plan (PDP) if they 
do not select a plan on their own. CMS enrolled about 5.5 million
dual-eligible beneficiaries in late 2005 and about 634,000 who	 
became dually eligible during 2006. GAO was asked to testify on  
(1) CMS&apos;s process for enrolling new dual-eligible beneficiaries  
into PDPs and its effect on access to drugs and (2) how CMS set  
the effective coverage date for certain dual-eligible		 
beneficiaries and its implementation of this policy. This	 
testimony is based on the GAO report, Medicare Part D: Challenges
in Enrolling New Dual-Eligible Beneficiaries (GAO-07-272).</abstract>
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<identifier type="preferred citation">GAO-07-1022T</identifier>
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<note>Testimony</note>
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 <searchTitle>GAO-07-1022T; Medicare Part D: CMS&apos;s Process and Policy for Enrolling New Dual-Eligible Beneficiaries;
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<subject>
 <topic>Beneficiaries</topic>
 <topic>Claims processing</topic>
 <topic>Eligibility determinations</topic>
 <topic>Health care programs</topic>
 <topic>Internal controls</topic>
 <topic>Medicaid</topic>
 <topic>Medicare</topic>
 <topic>Monitoring</topic>
 <topic>Pharmaceutical industry</topic>
 <topic>Prescription drugs</topic>
 <topic>Prospective payments</topic>
 <topic>Reimbursements</topic>
</subject>
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  <title>United States Statutes at Large</title>
  <partNumber>Volume 117 Page 2066</partNumber>
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 <identifier type="Statute citation">117 Stat. 2066</identifier>
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 <titleInfo>
  <title>United States Public Law 173 (108th Congress)</title>
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 <identifier type="public law citation">Public Law 108-173</identifier>
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