42 CFR 493, Subpart H - Participation in Proficiency Testing for Laboratories Performing Nonwaived Testing
- § 493.801 — Condition: Enrollment and testing of samples.
- § 493.803 — Condition: Successful participation.
- § 493.807 — Condition: Reinstatement of laboratories performing nonwaived testing.
- — Proficiency Testing by Specialty and Subspecialty for Laboratories Performing Tests of Moderate Complexity (Including the Subcategory), High Complexity, or Any Combination of These Tests
- § 493.821 — Condition: Microbiology.
- § 493.823 — Standard; Bacteriology.
- § 493.825 — Standard; Mycobacteriology.
- § 493.827 — Standard; Mycology.
- § 493.829 — Standard; Parasitology.
- § 493.831 — Standard; Virology.
- § 493.833 — Condition: Diagnostic immunology.
- § 493.835 — Standard; Syphilis serology.
- § 493.837 — Standard; General immunology.
- § 493.839 — Condition: Chemistry.
- § 493.841 — Standard; Routine chemistry.
- § 493.843 — Standard; Endocrinology.
- § 493.845 — Standard; Toxicology.
- § 493.849 — Condition: Hematology.
- § 493.851 — Standard; Hematology.
- § 493.853 — Condition: Pathology.
- § 493.855 — Standard; Cytology: gynecologic examinations.
- § 493.857 — Condition: Immunohematology.
- § 493.859 — Standard; ABO group and D (Rho) typing.
- § 493.861 — Standard; Unexpected antibody detection.
- § 493.863 — Standard; Compatibility testing.
- § 493.865 — Standard; Antibody identification.
Title 42 published on 2012-10-01
no entries appear in the Federal Register after this date.
This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.
This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].
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Title 42 published on 2012-10-01
The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to 42 CFR 493 after this date.
GPO FDSys XML | Text type regulations.gov FR Doc. 2013-02421 RIN 0938-AR49 CMS-3267-P DEPARTMENT OF HEALTH AND HUMAN SERVICES, Centers for Medicare & Medicaid Services Proposed rule. To be assured consideration, comments must be received at one of the addresses provided below, no later than 5 p.m. on April 8, 2013. 42 CFR Parts 416, 442, 482, 483, 485, 486, 488, 491, and 493 This proposed rule would reform Medicare regulations that CMS has identified as unnecessary, obsolete, or excessively burdensome on health care providers and suppliers, as well as certain regulations under the Clinical Laboratory Improvement Amendments of 1988 (CLIA). This proposed rule would increase the ability of health care professionals to devote resources to improving patient care, by eliminating or reducing requirements that impede quality patient care or that divert resources away from providing high quality patient care. This is one of several rules that we are proposing to achieve regulatory reforms under Executive Order 13563 on improving regulation and regulatory review and the Department's plan for retrospective review of existing rules.