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Clinical and Laboratory Standards Institute, 04/01/2003
Publisher: CLSI
File Format: PDF
$103.00$206.29
Published:01/04/2003
Pages:100
CLSI MM05A addresses guidelines for a variety of amplification-based laboratory tests, including polymerase chain reaction (PCR), transcription-based amplification system (TAS), strand displacement amplification (SDA), ligase chain reaction (LCR), and other methods now widely used in diagnostic hematopathology. This guideline provides a basis for laboratory implementation and quality assurance in this important area of diagnostic molecular medicine.
The U.S. Food and Drug Administration (FDA) has evaluated and recognized this approved-level consensus guideline for use in satisfying a regulatory requirement.
IT Security of In Vitro Diagnostic Instruments and Software Systems; Proposed Standard, AUTO11AE
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Autoverification of Clinical Laboratory Test Results; Approved Guideline, AUTO10AE
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Point-of-Care In Vitro Diagnostic (IVD) Testing; Approved Guideline, POCT4A2E
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