Multi-site Clinical Research

Jump on the fast track to better multi-site clinical data sharing practices and high impact trials

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Start Trials Faster

Establish shared stakeholder expectations on how to evaluate the readiness of a multi-site trial.

Better Quality Results

Increase the chance of real study impact with transparent, auditable, and managed data practices.

Reusable Framework

Build a repeatable and effective study structure to embed better practices for the future.

Unified Protocol for Multi-site RCTs

Experience the benefits of a repeatable framework for trustworthy data sharing across multi-site RCTs.

Initiate and Close with Confidence

Establish an evaluation framework to assess the readiness of multi-site RCTs.

Define shared expectations on what constitutes appropriate levels of analysis prior to formal trial closure.

Create Consistency and Respect Site Practices

Define shared sets of roles, activities, and network rules that factor individual site norms as well as industry standards.

Develop consistent execution of activities across sites. e.g. keeping similar control/treatment ratios to prevent false conclusions.

Develop Efficient Communication Protocols

Well designed and transparent channels of communications. Explicit understanding of how to receive clarification on protocols to protect study integrity.

Clearly defined process for multisite RCT decision making (i.e. required level of documentation, contrary views, review process)

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Our Multi-site Clinical Research solution provides a comprehensive, structured and streamlined process for managing the entire trial lifecycle.

Learn how to remove the friction and get better quality output for your next trial, and many trials beyond that!

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