Medidata’s Study Build experts understand what you are looking for in your protocol design. They have on average over 15+ years of industry experience and understand the need to blend clinical trial best practices with Medidata’s innovative technology to deploy the best possible design. We also understand the importance of working with your internal and external stakeholders to ensure proper integrations and data collaboration for a best-in-class study build.

There are times during a clinical trial when change is necessary. Medidata’s Study Build experts understand the challenges involved in a clinical trial rescue study and the importance of solid coordination between the Sponsor, CRO, and sites to minimize disruption. Our experts have migrated studies in all therapeutic areas, from small to large studies in every phase, and from any system. You can trust Medidata’s expertise and experience to make the changes safely and seamlessly.

Sponsors want ownership and control over their clinical data. That’s why Medidata provides you with a single source of data ownership for more comprehensive reporting and insights. Medidata experts work with your team to define and create standards resulting in reduced study build times, costs, and resource requirements. Access can also be granted to your CRO partners to reinforce standards and create efficiencies for faster study start-ups.