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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 
EO 13771 Designation: uncollected 
CFR Citation: 42 CFR 493   
Legal Authority: 42 USC 263a   
Legal Deadline:  None
Timetable:
Action Date FR Cite
NPRM  02/00/2011    
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