Fed Regist. 1992 Feb 28;57(40):7218-43.
These regulations set forth the rules for sanctions that HCFA may impose on laboratories that are found not to meet Federal requirements. These include the principal sanctions of suspending, limiting, or revoking the laboratory's certificate issued under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), and cancelling the laboratory's approval to receive Medicare payment for its services, and the alternative sanctions that may be imposed instead of or before the principal sanctions. These amendments are necessary to conform HCFA regulations to changes made in the law by the Omnibus Budget Reconciliation Act of 1987 (OBRA '87) and the 1988 amendments to section 353 of the Public Health Service Act (PHS Act). The latter are commonly referred to as "CLIA 88". The purpose of the amendments is to ensure that functioning laboratories are capable of providing accurate and reliable test results and that the health of individuals served by the laboratory and that of the general public is not adversely affected by laboratory operations and by testing procedures that do not meet the standards set forth in other subparts of part 493 of the HCFA regulations.
这些规定阐述了医疗保健财务管理局(HCFA)对被认定不符合联邦要求的实验室可能实施的制裁规则。这些制裁包括主要制裁措施,即暂停、限制或吊销根据1988年《临床实验室改进修正案》(CLIA)颁发给实验室的证书,取消实验室接受医疗保险支付其服务费用的批准,以及可在主要制裁措施之前或替代主要制裁措施而实施的替代制裁措施。这些修正案是为了使HCFA的规定符合1987年《综合预算协调法案》(OBRA '87)和《公共卫生服务法》(PHS法)第353条1988年修正案对法律所做的修改。后者通常被称为“CLIA 88”。修正案的目的是确保正常运作的实验室能够提供准确可靠的检测结果,并且实验室所服务的个人健康以及公众健康不会因不符合HCFA规定第493部分其他子部分所规定标准的实验室操作和检测程序而受到不利影响。