Карта сайта Интеллектуальная поисковая система
Добавить свою ссылку по ключевому запросуПоисковая система v3.kz поможет ускорить индексацию вашего сайта выводит в Топ
|
Карта сайта Интеллектуальная поисковая системаДобавить свою ссылку по ключевому запросуПоисковая система v3.kz поможет ускорить индексацию вашего сайта выводит в Топ |
|
|
described at 42 CFR § 493.20, Laboratories performing tests of moderate complexity: “subpart C or subpart D, and subparts F, H, J, K, M, and Q of this part... By Regulation – 42 CFR 493.15(c) for 9 generic tests (FOB, u. preg., u. dipstick, OTC glucose, spun hematocrit, ovulation, hemoglobin single analyte instrument, hemoglobin copper sulfate, and ESR)... 42 CFR 493.15(e)(1). Follow manufacturers instructions for performing the test. (42 CFR § 493.1281(a)) CLIA 15 PROFICIENCY TESTING • Each laboratory must enroll in a proficiency testing program that meets the criteria in subpart I. • At least twice annually... 4 42 CFR 493.15. 2 1 Proficiency Testing (PT) Programs CLIA requires laboratories to take ongoing measures to verify the accuracy of tests and procedures. (42 CFR 493.15(e).) You should state that any modification to the test or the manufacturer’s instructions will result in the test being classified as high complexity. 493.1850 Laboratory registry. 42 CFR Ch. IV (10–1–11 Edition) requirements are the same for Medicare approval as for CLIA certification. ї 493.2 Definitions. (42CFR493.1251) (42CFR493.15(e)(1)(2) Lab process adheres to manufacturer guidelines. Products currently used are matched to those in procedure manual. 42 CFR 493.15 (e) (1). 4. Dispose of swab into appropriate container. TEST PROCEDURE FOR SPECIMENS 1. Remove the test from the pouch and lay it on a flat surface. The implementing regulations are codified at 42 CFR Part 493. Информация взята v3.kz |
|
|
|
загрузка...
|