3 edition of Clinical laboratory improvement act of 1978 found in the catalog.
Published
1978
by U.S. Govt. Print. Off. in Washington
.
Written in English
| Classifications | |
|---|---|
| LC Classifications | KF27 .W344 1978 |
| The Physical Object | |
| Pagination | iv, 101 p. ; |
| Number of Pages | 101 |
| ID Numbers | |
| Open Library | OL4375471M |
| LC Control Number | 78603237 |
Clinical Laboratory Improvement Amendments of (CLIA ’88). We hope that you will find it helpful in answering many of your questions regarding regulations for clinical laboratory testing. These CLIA regulations are far-reaching, and now regulate physician-office laboratory through the Omnibus Budget Reconciliation Act of (OBRA. List seven regulations of the Clinical Laboratory Improvement Act (CLIA) that apply to the clinical medical assistant performing urine testing. 1. Appropriate training in the methodology of the test being performed.
H.R. (94th). A bill to amend the Public Health Service Act and the Social Security Act to revise and improve the authorities under those acts for the regulation of clinical laboratories. In , a database of bills in the U.S. Congress. TOPN: Clinical Laboratories Improvement Act of | A | B | C Act') or by invoking public outrage or sympathy (as with any number of laws named for victims of crimes). History books, newspapers, and other sources use the popular name to refer to these laws. Clinical Laboratories Improvement Act of Pub. L. ,Sec 5, Dec.
nonprofit organization that sets standards and guidelines under the Clinical Laboratory Improvement Act Clinical Lab Improvement Act of (CLIA '88) Federal law that mandated regulation of all facilities that performed patient testing. Clinical Lab Improvement Act of What are the primary lab accrediting organizations. COLA CAP TJC. The primary lab accrediting organizations have the authority to. Enforce CLIA ' Name three components of CLIA ' Levels of testing complexity Training of personnel Credentialing required.
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Clinical laboratory improvement act of report by United States. Congress. House. Committee on Interstate and Foreign Commerce; United States. Congress. House. Committee on Ways and Means; United States. Congressional Budget OfficePages: Get this from a library. Clinical laboratory improvement act of report.
[United States. Congress. House. Committee on Interstate and Foreign Commerce.]. The Clinical Laboratory Improvement Amendments of statute is an amendment to the Public Health Services Act in which Congress revised the federal program for certification and oversight of clinical laboratory testing.
Two subsequent amendments were made after The law continues to be cited as CLIA ’88 as named in legislation. Get this from a library. H.R.Clinical Clinical laboratory improvement act of 1978 book improvement act of explanation, justification, and comparison with present law.
[United States. Congress. House. Committee on Ways and Means. Subcommittee on Health.]. Shortly after the first edition of this book appeared, the U.S. Congress passed the so-called Clinical Laboratory Improvement Act (CLIA), in reaction to some tragic consequences of false-negative Pap smears that had been performed, ironically, in federally regulated clinical laboratories.
The Clinical Laboratory Improvement Amendments of (CLIA) regulations include federal standards applicable to all U.S. facilities or sites that test human specimens for health assessment or to diagnose, prevent, or treat disease.
Refer to the Related Links Outside CMS section below for the following information concerning the Clinical Laboratory Improvement Amendments (CLIA) regulations: The most current version of the CLIA regulations Partincluding all changes through 5/12/ Search a database of documents related to CLIA from these sources: is a codification (arrangement) of the general and permanent final rules published in the Federal Register by the executive departments and agencies of the Federal Government.
is the official daily publication for notices, proposed rules, and final rules published by federal. In total, CLIA covers approximatelylaboratory entities. The Division of Clinical Laboratory Improvement & Quality, within the Quality, Safety & Oversight Group, under the Center for Clinical Standards and Quality (CCSQ) has the responsibility for implementing the CLIA Program.
M uch of the history of the clinical lab dur- ing the last 30 years can be described as a reaction to the development of Medicare and Medicaid, as well as to the regulatory bodies that were established to oversee the administration of these Size: KB.
Feb 9, H.R. (95th). A bill to amend the Public Health Service Act to revise and strengthen the program under that Act for national standards for and licensing of clinical laboratories, to amend the Social Security Act to require laboratories providing services financed under titles XVIII and XIX of such Act to meet the requirements of such program, and.
Clinical Laboratory Improvement Act - Amends the Public Health Service Act to direct the Secretary of Health, Education, and Welfare to promulgate national standards for clinical laboratories.
Defines the terms "laboratory" and "clinical laboratory" for purposes of this Act. I have benefitied greatly from this well thought out and clearly presented guide to the use of laboratory studies in clinical practice.
Unlike other guides which are mainly compendiums of various lab tests as they relate to given diseases, Dr. Ravel's work provides physiolgic/pathophysiologic explanations both as a background for understanding indications for laboratory /5(2).
The Clinical Laboratory Improvement Amendments (CLIA) of are United States federal regulatory standards that apply to all clinical laboratory testing performed on humans in the United States, except clinical trials and basic research.
Clinical laboratory improvement act of hearing before the Subcommittee on Health of the Committee on Ways and Means, House of Representatives, Ninety-fifth Congress, second session, on H.R. May 9, CLIA is the Clinical Laboratory Improvement Amendments of It is an amendment to the original Clinical Laboratory Improvement Act of The purpose of CLIA ‘88 is to provide site-neutral quality (accuracy, reliability, and timeliness) of.
The summary below was written by the Congressional Research Service, which is a nonpartisan division of the Library of Congress. 7/12/Reported to House amended, Part III. (Reported to House from the Committee on Ways and Means with amendment, H.
Rept. Clinical Laboratory Improvement Act (CLIA) Also called Clinical Laboratory Improvement Amendments. Federal statute passed in that established minimum quality standards for all laboratory testings.
Clinical Laboratory Improvement Act. The New Mexico Clinical Laboratory Improvement Act (CLIA) program ensures that all laboratory facilities (including physician office laboratories) meet the established health and safety standards for specimen mission of the program is to ensure that the highest quality of laboratory testing is performed in New Mexico through.
NOTE: Congress passed the Clinical Laboratory Improvement Amendments (CLIA) in establishing authority to promulgate standards for certain laboratory testing to ensure the accuracy, reliability and timeliness of test results regardless.
CLIA; Clinical Laboratory Improvement Act of [P.L. ]: To implement CLIA, section 5(a) Part F of title III of the Public Health Service (PHS) Act (42 U.S.C. ) was amended by the changing the title to read: “Licensing -- Biological Products and Clinical.CLINICAL LABORATORY IMPROVEMENT AMENDMENTS (CLIA) APPLICATION FOR CERTIFICATION.
I. GENERAL INFORMATION. laboratory is accredited by for CLIA purposes, or for which you have applied for accreditation for CLIA purposes.
Any person who intentionally violates any requirement of section of the Public Health Service Act asFile Size: KB.Regulations for Implementing the Clinical Laboratory Improvement. Amendments of A Summary.
InCongress passed the Clinical Laboratory Improvement Amendments (CLIA), which set standards to improve the quality of clinical laboratory testing in all laboratories in the nation that conduct testing on human specimens for health.
