Edge Trial Planning and Management

One platform for Clinical Operations.


Solve for patient scarcity with cross-sponsor analytics that optimize protocol design and feasibility


Automate payments to sites within 30 days of activity – and become sites’ “sponsor of choice”


Modernize study management with full ICH E6 (R2) GCP compliance and TMF automation

Our Solutions Have Proven Value

Edge Study Design and Feasibility

31% Lower Protocol Complexity with 50% More High-Performing Sites

Optimize protocol design to lower patient burden, and find the sites that have historically performed best in similar therapeutic areas and geographies.
Site and Payments

80% Faster Study Setup and 60% Faster Payment Cycle Times

Sites say their top pain point is getting paid on time. You can automatically calculate, approve and disburse payment in 100+ countries as soon as a procedure is entered into an EDC.

95% Compliance of TransCelerate Requirements

Conform with the latest ICH GCP monitoring guidelines worry free. Get early, real-time and unique insights, strengthen cross-functional team collaboration and provide greater workflow efficiency and reduce the administrative burden on CRAs.
EDGE CTMS, Clinical Trials

40% Better Visit Reporting Productivity

Discover the next generation of clinical operations by taking a modular approach that allows you to choose the right mix of study management, automated payments, and strategic monitoring.
Edge eTMF, simplify filing regulated content

76% TMF Automated

Simplify the filing of what can be 100K+ documents by automating the input of up to 76% of TMF artifacts.

Customer Stories

"Edge Payments stood out as a true end-to-end solution, and for its ability to reimburse sites quickly and accurately by directly integrating with Rave EDC– important as we invest in processes and technology that help us continue to stand out as a top-ranked performer for service and customer loyalty.”
Anthony Doyle , Chief Financial Officer, Worldwide Clinical Trials
How we Helped
“Having our documentation in a secure, validated environment enables an ease of use for authoring, review, and approval. This allows us to pay attention to other things so we can focus on our product development.”
Hayley Lewis, VP Regulatory & Compliance, Zosano Pharma
How we Helped
"We needed to find a trusted partner to work with us, to grow with us AND deliver and provide innovative technology solutions for our clinical trials, we found that partner in Medidata."
Laurie Callan, Director of Clinical Data Management, TESARO
How we Helped

Additional Solutions


Rave to power today’s targeted therapies—all of the data, all of the protocols, all of the workflows—in one place.


Embed predictive analytics for every clinical development decision to identify red flags sooner through MEDS & AI