| 000 | 03091nam a22003257i 4500 | ||
|---|---|---|---|
| 008 | 251127t20252025njua|||| i||| 001 0 eng | ||
| 020 |
_a9781683674450 _qhardback _cRM385.89 (PRAKLINIKAL) |
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| 040 |
_aDNLM/DLC _erda _beng _dUKM |
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| 090 |
_aQY70 _b.M379t 2025 9HUKMPRA |
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| 100 | 1 |
_aMartin, Rebekah M., _eauthor. |
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| 245 | 1 | 0 |
_a101 topics for clinical microbiology laboratory leaders : _baccreditation, verification, quality systems, and more / _cRebekah M. Martin. |
| 246 | 1 | _aOne hundred and one topics for clinical microbiology laboratory leaders | |
| 264 | 1 |
_aWashington, DC : _bASM Press, _c[2025]. |
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| 264 | 4 | _c©2025. | |
| 336 |
_atext _2rdacontent |
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| 337 |
_aunmediated _2rdamedia |
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| 338 |
_avolume _2rdacarrier |
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| 504 | _aIncludes bibliographical references and index. | ||
| 505 | _aClinical Laboratory Improvement Amendments (CLIA) and Regulatory Oversight -- Clinical Laboratory Improvement Amendments (CLIA) Certificates -- Waived Testing -- Laboratory Accreditation -- Verification and Validation -- Performance Characteristic : Precision -- Performance Characteristic : Accuracy/Agreement -- Performance Characteristic : Reportable Range -- Performance Characteristic : Reference Interval -- Performance Characteristic : Analytical Sensitivity -- Performance Characteristic : Analytical Specificity -- Additional Performance Characteristics -- Unacceptable Results and Resolution -- Documentation for Verification and Validation Studies -- Quality Management Systems -- Essential : Organization -- Essential : Laboratory Personnel -- Essential : Customer Service -- Essential : Facilities and Safety -- Essential : Purchasing and Inventory -- Essential : Equipment -- Essential : Process Control -- Essential : Document and Records Management -- Essential : Information Management -- Essential : Occurrence Management -- Essential : Assessment -- Essential : Process Improvement. | ||
| 520 | _a"Laboratory accreditation is a vital and necessary process for clinical laboratories, and the requirements coming from the oversight bodies, CAP, CLIA, and FDA. And although information are freely accessible, they are often confusing and difficult to execute in the lab. Every clinical microbiology laboratory director, manager, and supervisor must interpret the requirements and work to keep the laboratory in compliance while responding to novel microbe outbreaks in addition to the regular workflow of testing. This resource gathers information from many different sources into one place and addresses the "how-tos" of implementing regulations around laboratory activities"--cProvided by publisher. | ||
| 650 | 2 |
_aLaboratories, Clinical _xstandards. |
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| 650 | 2 |
_aMicrobiological Techniques _xstandards. |
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| 650 | 2 |
_aAccreditation _xstandards. |
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| 651 | 2 | _aUnited States. | |
| 942 |
_2lcc _n0 |
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| 949 | _o101033246 | ||
| 991 | _aJabatan Mikrobiologi, Praklinikal | ||
| 999 |
_c693540 _d693540 |
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