Equipping Primary Care, Urgent Care and Independent Pharmacies with a proprietary PCR technology for in-clinic, Antibiotic Resistance syndromic testing
Our proprietary molecular PCR reagents were strategically crafted with the intention to create a clinically superior offering that was financially sustainable for the "long-haul", all processed on one economical machine.
In today's volatile market of ever-changing reimbursement, patient behavioral patterns, new technologies and M&A transactions, our proprietary technology minimizes risk of investment in order to thrive during all aforementioned market challenges.
With on-site validation studies run for every single organism on every single panel, our technology boasts 99% or higher accuracy, specificity, sensitivity and precision.
Outfitted on a common, "workhorse"-type thermal cycler, our proprietary PCR reagents have proven to provide for an elevation of patient care, an increase in laboratory and clinic efficiencies, as well as dramatically boosting positive revenue cycles.
35 Organisms
Process 2 patients in 1 hour
Sensitivity: 99.52%
Made in America
Time to detection:
63-90 minutes
19 Organisms
9 Antibiotic Resistance Markers
Process 4 patient in 1 hour
33 Organisms
Process 3 patients in 1 hour
15 Organisms
Process 2 patient in 1 hour
19 Organisms
9 Antibiotic Resistance Markers
Process 4 patient in 1 hour
All of our proprietary panels are validated on-site by one of our scientists with data and results far exceeding FDA requirements.
We validate every single organism, on every single panel and provide all clinical and analytical validation data that is necessary.
On-site setup, validation and training takes roughly 5 days to fully complete, which includes all current and desired panels.
New and Increased Revenue Stream
Faster Turn-Around-Time by processing specimens on-site
Faster Treatment Plan, Better Clinical Outcomes
Manage In-Network Billing
Antibiotic Resistance Stewardship
Consulting for High Complexity Laboratory License
Assist in identifying appropriate lab personnel
All equipment and ancillary items to properly process tests
5 Day On-Site Installation, Validation and Training
Choose which test panels would be appropriate
Review and sign agreement
Work with us to complete and submit CLIA licenses
5 day on-site training and validation completed
Clinical and technical data signed off by Laboratory Director
Once Laboratory Director approves, lab is ready to start