Fed Regist. 1990 Mar 14;55(50):9538-610.
This rule revises regulations for laboratories regulated under the Medicare, Medicaid and Clinical Laboratories Improvement Act of 1967 (CLIA '67) programs. The revisions recodify the regulations for these programs into a new part 493 in order to simplify administration and unify the health and safety requirements for all programs as much as possible. We will now have a single set of regulations for the three programs, with an additional subpart for the licensure procedures unique to the CLIA program. We are revising the regulations to remove outdated, obsolete and redundant requirements, make provision for new technologies and place increased reliance on outcome measures of performance. We provide for new uniform proficiency testing standards. We have also added requirements for additional specialties, such as clinical cytogenetics. We also implement the now and self-implementing provisions of the Clinical Laboratory Improvement Amendments of 1988 (CLIA '88).
本规则修订了依据1967年《医疗保险、医疗补助和临床实验室改进法案》(CLIA '67)项目进行监管的实验室的相关规定。这些修订将这些项目的规定重新编入新的第493部分,以简化管理并尽可能统一所有项目的健康与安全要求。现在,我们将为这三个项目制定一套统一的规定,并为CLIA项目特有的许可程序增设一个子部分。我们正在修订规定,以去除过时、陈旧和冗余的要求,为新技术提供规定,并更多地依赖绩效结果指标。我们制定了新的统一能力验证标准。我们还增加了对其他专业领域的要求,如临床细胞遗传学。我们还实施了1988年《临床实验室改进修正案》(CLIA '88)中即时生效和自行实施的条款。