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5 panel multi line drug test card
The Rapid Multi-Drug Test is a lateral flow chromatographic immunoassay for the qualitative detection of multiple drugs and drug metabolites in urine.
The Rapid Screen Multi-Drug Test is an immunoassay based on the principle of competitive binding. Drugs, which may be present in the urine specimen, compete against their respective drug conjugate for binding sites on their specific antibody.
QUALITY CONTROL
An internal procedural control is included in the test device.
A line must form in the Control band region regardless of the presence or absence of drugs or metabolites. The presence of the line in the Control region
indicates that the proper sample volume has been used and that the reagents are migrating properly. If the line in the Control region does not form,
the test is considered invalid.
To ensure proper kit performance, it is recommended that the test devices be tested once a week with external controls. External controls are available from
commercial sources. It is important to make sure that the control values are within established limits. If the values of external control do not fall within established
limits, the test results are invalid. Additional controls may be tested according to guidelines or requirements of local, state, and/or federal regulations or
accrediting organizations.
LIMITATIONS OF PROCEDURE
• The assay is designed for use with human urine only. • A positive result with any of the tests indicates only the presence of a drug/metabolite and does not indicate or measure intoxication.
• There is a possibility that technical or procedural error as well other substances as factors not listed may interfere with the test
and cause false results. See SPECIFICITY for lists of substances that will produce positive results, or that do not interfere with test performance. • If adulteration is suspected, the test should be repeated with new sample.
PERFORMANCE CHARACTERISTICS
Accuracy - The accuracy of the Rapid Exams Dip card was evaluated in comparison to commercially available drug screen tests. Sixty (60) negative
urine samples collected from presumed non-user volunteers were tested by both Rapid Exams Dip card and commercially available drug screen tests.
Of these negative urine samples tested, all were found negatives by both methods. In a separate study, positive urine samples,obtained from clinical laboratories
where the drug concentrations were determined by GC/MS (TCA concentrations were determined by HPLC), were tested by Rapid Exams Dip card and commercial drug screen tests.
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