CROs & Partners
A modern evidence platform for CRO delivery teams
Design, build, and deliver clinical studies using a flexible, easy-to-use evidence platform — while strengthening sponsor relationships and delivery margins.
CROs and partners face increasing pressure
CROs and specialist partners are expected to deliver faster, more efficiently, and with greater transparency — often while working across multiple sponsor systems and fragmented technology stacks.
Do you relate to any of the following challenges?
Delays caused by third-party EDC build and change requests
Margin pressure from outsourced or inflexible data platforms
Limited visibility and control over evidence workflows
Sponsor expectations for speed, quality, and audit readiness
Differentiating services in a competitive delivery landscape
How Ledidi supports CROs and partners today
Ledidi is a modern, intuitive evidence platform that CROs can use directly to build, manage, and deliver studies — without relying on slow or costly third-party EDC vendors.
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Build and manage EDC in house
Configure studies, variables, and data capture workflows directly in Ledidi. Reduce dependency on external vendors, shorten timelines, and keep EDC build under your control.
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Deliver faster and respond to change
Ledidi’s flexible, low-friction setup allows CRO teams to adapt studies quickly as protocols evolve — reducing delays, rework, and sponsor frustration.
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Improve margins and predictability
By bringing evidence workflows in house, CROs can reduce external costs, streamline delivery, and improve commercial predictability across studies.
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Increase sponsor trust and transparency
Provide sponsors with real-time visibility into study progress and data quality, supporting stronger relationships and repeat business.
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Use a platform teams actually enjoy using
Ledidi is designed for day-to-day use by CRO project teams, data managers, and monitors — prioritising usability, clarity, and speed without compromising compliance.
Validation and audit ready
Ledidi Trials has successfully completed an independent audit confirming its readiness for use in GxP-regulated clinical studies. The assessment verifies compliance with key regulatory expectations, including FDA 21 CFR Part 11, ICH GCP E6(R3), and ISPE GAMP 5.
Ledidi also provides a Validation Package to CROs and partners to help streamline the validation obligations.
An emerging partnership ecosystem
Ledidi is actively building a partner ecosystem to support sponsors with end-to-end evidence generation — combining a modern evidence platform with experienced delivery partners.For CROs and specialist providers, this creates opportunities to:
Engage earlier with sponsors using Ledidi
Deliver services around a shared, sponsor-trusted platform
Access new clients looking for integrated evidence solutions
We welcome conversations with CROs and partners interested in shaping this ecosystem together.
Designed to fit alongside your delivery model
Ledidi integrates with existing clinical operations, monitoring, and analytics processes.CROs can adopt the platform incrementally — using it where it adds most value — without reengineering established delivery models.
