![]() Photos displayed are for illustrative purposes only. Your use of this website and the information contained herein is subject to our Website Terms and Conditions and Privacy Policy. The products and information contained herewith may not be accessible in all countries, and Abbott takes no responsibility for such information which may not comply with local country legal process, regulation, registration and usage. This website is governed by applicable U.S. No use of any Abbott trademark, trade name, or trade dress in this site may be made without the prior written authorization of Abbott, except to identify the product or services of the company. Unless otherwise specified, all product and service names appearing in this Internet site are trademarks owned by or licensed to Abbott, its subsidiaries or affiliates. Ensuring the proper development and implementation of a QCP.Ensuring that the RA considers both the CLIA requirements for accurate and reliable test results and that test result quality is appropriate for patient care.Considering the laboratory’s clinical and legal responsibility for providing accurate and reliable patient test results prior to implementing a QCP that is less stringent than the specified Analytic Systems control regulations listed in the CLIA IQCP interpretive guide table “Eligibility for IQCP”.Deciding whether a laboratory will seek to meet its CLIA QC obligations through IQCP, and, if they decide to do so, ensuring that the QCP they develop meets the IQCP requirements. ![]() ![]() Ensuring that QC and QA programs are established and maintained to assure the quality of laboratory services, including the identification of failures in quality as they occur.Per the CLIA IQCP interpretive guide, the Laboratory Director is responsible for: ![]()
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