De-Risk Your Clinical Studies
Unmatched visibility and control enable you to complete studies on-time, on budget, and with high data integrity.
Sponsors deserve a better CRO experience
Pharma, biotech, and medical device sponsors (in all therapeutic areas) need a Contract Research Organization (CRO) that provides more control over the planning, funding and execution of clinical studies.
You need visibility and control over:
- Costs
- Timelines
- Recruitment/Enrollment/Engagement
- Data Collection and Management
- Regulatory Compliance
- Variables Affecting On-Time Database Lock
You need more than a CRO…
You need a true business partner
It’s not enough to just conduct a study to bring your product to market. You want to collect the data necessary for regulators, plus capture secondary data to inform your successful commercial strategy. Having a partner who can plan and execute compliant clinical studies, integrating strategic commercial counsel, helps you maximize the value of your study.
Our clients enjoy the way we:
- Contract for services on a fixed-cost model, plus pass-throughs, minimizing change orders
- Model and validate study plans to match investment needs
- Collaborate, design, and execute on sponsor-approved, protocol-specific flight plans
- Use automation to optimize recruitment, enrollment, engagement, and data collection
- Reduce data management and personnel-related costs by 50-70%
