Medical Device & Diagnostic Study Execution
Alchemy Trials specializes in the coordination and execution of mainly low-risk medical device clinical research. We facilitate the testing of innovative diagnostic technologies within primary care settings to support advancements in patient care and medical technology.
Expert Coordination for Non-Invasive Clinical Research
Our organization focuses on low-risk, noninvasive medical device studies that require minimal procedural participation from the Medical Director. We have extensive experience executing protocols for common diagnostic tools, such as rapid tests for Influenza A, RSV, and COVID-19, ensuring that all procedures are conducted with precision by our trained personnel.
What types of medical devices do you typically test?
We specialize in low-risk, non-invasive medical devices, particularly rapid diagnostic tests for respiratory infections like Influenza, RSV, and COVID-19.
Does my practice need to provide any special equipment?
No, Alchemy Trials and the study sponsors provide all necessary protocol-specific materials and devices required for the study.
What is the clinical risk for my practice and patients?
Because we focus on non-invasive devices, there is extremely low to no clinical risk for the practice.
Who is responsible for performing the study procedures?
Study protocols are executed entirely by Alchemy-trained research personnel deployed to your clinic.
What involvement is required from the Medical Director?
The Medical Director provides oversight, but the specialized research tasks are handled by our staff to minimize your burden.
Are these studies usually permanent additions to the clinic?
These are typically short-term studies, with a standard completion timeframe of approximately 8 to 12 weeks.
