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HHS/CMS | RIN: 0938-AT56 | Publication ID: Fall 2019 |
Title: Clinical Laboratory Improvement Amendments (CLIA) Fees (CMS-3356-P) | |
Abstract:
This proposed rule follows the notice with comment published on December 31, 2018. This rule would update fees for determination of program compliance and additional fees for laboratories established under the Clinical Laboratory Improvement Amendments (CLIA) regulations as well as the collection of other fees we are authorized to collect, such as fees for revised certificates, post survey follow-up visits, complaint investigations, and activities related to imposition of sanctions. |
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Agency: Department of Health and Human Services(HHS) | Priority: Other Significant |
RIN Status: Previously published in the Unified Agenda | Agenda Stage of Rulemaking: Long-Term Actions |
Major: No | Unfunded Mandates: No |
EO 13771 Designation: Other | |
CFR Citation: 42 CFR 493 | |
Legal Authority: 42 U.S.C. 263a |
Legal Deadline:
None |
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Timetable:
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Regulatory Flexibility Analysis Required: Undetermined | Government Levels Affected: Undetermined |
Federalism: No | |
Included in the Regulatory Plan: No | |
RIN Data Printed in the FR: No | |
Agency Contact: Jessica Wright Health Insurance Specialist Department of Health and Human Services Centers for Medicare & Medicaid Services Center for Clinical Standards and Quality, MS: C2-21-16, 7500 Security Boulevard, Baltimore, MD 21244 Phone:410 786-3838 Email: jessica.wright@cms.hhs.gov |