Doing good by doing well.
Providing solutions in the clinical research industry.
The clinical research environment is inefficient. Sponsors, CROs, and sites spend excessive time and resources maintaining clinical sites.
We streamline the process by using our experience and platforms to do the heavy lifting in an efficient manner, meeting everyone's needs.
Navigating a complex industry is no problem.
32
SITES
26
INVESTIGATORS
63
TRIALS
14
INDICATIONS
Study Recruitment
We use our experience and network to find studies that best fit our investigator's interest while compiling all trainings on secured platforms for easy access.
We manage all regulatory documents from start-up to close-out, making sure that Sponsors & CROs have access to documents in a time-efficient manner.
Regulatory Management
Protocol & Data Management
We provide trainings on protocols, EDCs, and IWRSs while managing financial, visit tracking, and electronic data collection. We are fully paperless!
We send highly qualified staff to conduct the study at a physician's own clinic. We are so confident in our team that we require CCRP certifications once eligible.
Resources & Personnel
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Lundbeck
Sponsors we've worked with:
Our Sites
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