Oncobiomix, a fast-growing startup specializing in microbiome-based prostate cancer diagnostics, knew they faced a challenge. Running a decentralized clinical trial with multiple vendors for eConsent, EDC, and ePRO was an open invitation for spiraling costs and disorganized data.
In this exclusive case study, you’ll learn how Oncobiomix consolidated their entire trial process—consent forms, patient surveys, sample tracking, and data capture—into one streamlined platform. With a single study coordinator, they saved $100K in potential staffing fees and achieved near-perfect questionnaire completion.
We won’t reveal all the specifics here, but the story goes beyond cost savings. It offers insight into:
- How Oncobiomix maintained FDA-ready documentation
- The secret to real-time data monitoring without missing endpoints
- The impact of automated alerts and simplified workflows
If you’re tired of juggling multiple tools or risking half-finished surveys, the Oncobiomix approach could be your blueprint for success. Download the full case study to see how a focused, all-in-one method can help you meet patient needs, save valuable resources, and keep you miles ahead of compliance demands.
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