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Respiratory Panel Point of Care Study Request

We aim to demonstrate the clinical utility of our near patient respiratory testing solutions by generating real world evidence. Our goal is to conduct two studies during the respiratory season within an urgent care and general practice clinic. Conducting studies in the point of care setting can be challenging as sites may lack the research experience and logistical support to do so. We are seeking motivated researchers to partner with in this setting who have experience conducting research studies. Priority will be given to those sites who currently have administrative support in place to manage study operations and logistics.

RFP Details
Respiratory Panel
• Non-Clinical Patient Impact: days of work/school missed, satisfaction/acceptance of diagnosis and treatment plan, impact on expectations of symptoms and disease course, return visits and follow-up care, patient experience evaluation metrics
• Clinician Care Delivery: communication of results and plan of care, change in diagnosis, change in prescribing patterns, interpretation of report, overall experience vs current standard of care/competitors/send out testing
• Clinical Outcomes: impact on ability to aid in diagnosis, use of antimicrobials prescribing, and antibiotic related patient safety
• Clinical Utility: healthcare utilization, impact on patient management, ancillary testing, workflow measures
• Public and population impact: overall healthcare resource utilization, cost vs comparator testing, workflow, compliance with joint commission accreditation standards for ambulatory care settings

•   Clinic must have a moderately complex lab or clia waived lab
•   Must have a feasible comparator arm (site cannot solely use RP2.1)
•   Need not be a current BioFire customer
•   Experience conducting research with a support team in place
•   Proven track record of publishing papers

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