Choosing The Right Protocol, Personnel and Research Institution
Product and therapy validation as mandated by the various oversight organizations (FDA, CDC, etc.) starts with the design of a carefully controlled study process. Before that happens, the product or therapy has to demonstrate patient efficacy and market credibility to make sure we are going down the right path. That process starts with empirical and anecdotal work to align all trial work to everyone’s goal: a validated and certified product that is safe and works.
Hark Health Services has extensive experience with the design and implementation of empirical, anecdotal, IRB, and RCT trials with the most prestigious research labs and teaching hospitals in the country, including Sloan Kettering, Duke, UNC Vascular, Stanford, Mayo Clinic, and Cleveland Clinic, to reference a few, but we have national connections with many others.
Labs, research hospitals, and trial personnel offer varied and diverse choices across the country for medical product entrepreneurs. We lead and manage parts of or the entire process of prime investigator reviews and produce relevant histories of research institutions and ultimate results in publishable posters and papers. This process is involved and can get caught in over-deadline and over-budget situations quickly. Hark Health Services has over fifteen years of experience in managing this process, choosing the right personnel and partners to successfully achieve everyone’s desired results in a faster-than-average time frame.