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HHS/CMS | RIN: 0938-AQ38 | Publication ID: Fall 2010 |
Title: ●Medicare, Medicaid, and CLIA Programs; PatientÂ’s Access to Laboratory Test Report (CMS-2319-P) | |
Abstract: This proposed rule would revise portions of the Clinical Laboratory Improvement Amendments of 1988 (CLIA) to clarify existing policy, promote patient access to laboratory test reports and establish electronic health records. | |
Agency: Department of Health and Human Services(HHS) | Priority: Other Significant |
RIN Status: First time 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 |
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 | |
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 |