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《临床实验室改进法案》项目费用收取——医疗保健财务管理局。带评论的最终规则。

Clinical Laboratory Improvement Act program fee collection--HCFA. Final rule with comment.

出版信息

Fed Regist. 1992 Feb 28;57(40):7188-218.

Abstract

This rule implements provisions of section 353 of Public Health Service Act (as amended by the Clinical Laboratory Improvement Amendments of 1988). Those provisions require laboratories to pay fees for issuance of registration certificates, certificates of waiver, certificates of accreditation, or certificates and to fund activities to determine compliance with the requirements established by the Department of Health and Human Services for laboratory testing. It also establishes the policy that laboratories licensed by and located in States with licensure programs approved by HHS may be exempt from the requirements of the Clinical Laboratory Improvement Amendments of 1988 (CLIA). This rule also establishes the methodology used to determine the amount of the fees charged for certificates of waiver, registration certificates, certificates of accreditation, or certificates and activities to establish application procedures and determine compliance with applicable certification requirements.

摘要

本规则实施了《公共卫生服务法》第353条的规定(经1988年《临床实验室改进修正案》修订)。这些规定要求实验室支付颁发注册证书、豁免证书、认可证书或其他证书的费用,并为确定是否符合卫生与公众服务部制定的实验室检测要求的活动提供资金。它还确立了一项政策,即由卫生与公众服务部批准的有许可计划的州颁发许可且位于这些州的实验室可免于遵守1988年《临床实验室改进修正案》(CLIA)的要求。本规则还确立了用于确定豁免证书、注册证书、认可证书或其他证书以及确立申请程序和确定是否符合适用认证要求的活动所收取费用金额的方法。

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