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| HHS/CMS | RIN: 0938-AQ38 | Publication ID: Spring 2011 |
| Title: Medicare, Medicaid, and CLIA Programs; Patient Access to Laboratory Test Reports (CMS-2319-P) | |
| Abstract: This proposed rule would revise portions of the Clinical Laboratory Improvement Amendments of 1988 (CLIA) to clarify existing policy,and promote patient access to laboratory test reports. | |
| Agency: Department of Health and Human Services(HHS) | Priority: Other Significant |
| RIN Status: Previously published in the Unified Agenda | Agenda Stage of Rulemaking: Proposed Rule Stage |
| Major: Undetermined | Unfunded Mandates: No |
| CFR Citation: 42 CFR 493 | |
| Legal Authority: 42 USC 263a | |
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Legal Deadline:
None |
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Timetable:
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| Regulatory Flexibility Analysis Required: Undetermined | Government Levels Affected: Undetermined |
| Small Entities Affected: Businesses, Governmental Jurisdictions | Federalism: No |
| Included in the Regulatory Plan: No | |
| RIN Data Printed in the FR: No | |
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Agency Contact: Judith Yost Director, Division of Laboratory Services Department of Health and Human Services Centers for Medicare & Medicaid Services S-2-09-27, Center for Clinical Standards and Quality, Mail Stop C2-21-16, 7500 Security Boulevard, Baltimore, MD 21244-1850 Phone:410 786-3531 Email: judith.yost@cms.hhs.gov |
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