PECRKO Research is in the database development phase currently. Upon completion of our database, we will provide our database to research providers to connect local vetted participants.
To solve the low research participation rate, PECRKO Research provides clinical/pharmaceutical research education and a research participant database.
PECRKO Research provides virtual research education to all citizens, yet we focus our efforts on the minority community. Minorities include African Americans/Black, Hispanics, Asian, Native Americans, Pacific Islanders and Veterans. The goal of this education is to provide information on the advancements that all citizens, but especially the minority community, can provide to clinical/pharmaceutical research and how PECRKO Research works to support this advancement.
We then connect citizens to local research providers: physician offices, research firms, hospitals, university students, Clinical Research Organizations (CRO), Bio/Tech and Pharmaceutical companies.
Through customer discovery we have affirmed that minorities are concerned with ways to support their health and the health of their family and friends. Yet, they are unlikely to participate in clinical research without adequate education from a trusted source. PECRKO Research is that trusted source.
When more minorities participate in research it can change the way that medications are designed, which can support better medical care and less medical expenses.
We are unique, as we have minority participants within our database; we educate minorities about the benefits in participating in clinical/pharmaceutical research, which supports their continued contribution to clinical/pharmaceutical research; we offer an incentive to our minority participants to support their patronage in PECRKO Research for research connectivity; and, we have a competitive advantage because our database subscriptions prices are at a lower cost.
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