Specifications include, but are not limited to: 1. Be fully automated with minimal technician operation or assistance needed after the beginning of analysis. 2. Capable of providing consistent results with an option to retrieve archived data. 3. Capable of Laboratory Information Management System (LIMS) integration with the established system at the ASCL. 4. Bar-code reader enabled. 5. Capable of providing semi-quantitative data with a minimum seven (7) point calibration curve and user definable multipoint rules for quality control. 6. The analytical process must not be greater than one (1) hour and fifteen (15) minutes of incubation time when analyzing an estimated 90 samples per hour for multiple drug classes. 7. Capable of conducting analysis on the follow: a. Whole blood, post-mortem blood, urine, oral fluid, vitreous humor hair meconium, and tissue. b. Synthetic blood and urine for validation purposes. c. Utilizing less than one milliliter of whole sample without dilution.
