Webinar: The Benefits of a Seamless IRT and EDC Integration in Clinical Trial Execution

Webinar: The Benefits of a Seamless IRT and EDC Integration in Clinical Trial Execution

There’s a lot of discussion around the benefits of a unified platform, or one-stop-shop for eClinical solutions (Electronic Data Capture [EDC], Interactive Response Technology [IRT], eConsent, electronic Patient-Reported Outcomes [ePRO], etc.). While a single platform may satisfy the needs of smaller studies, what happens when your studies become larger and your protocols become more complex? Increasing complexities often force study teams to start looking for multi-vendor approaches.

Two software companies, Veeva Systems and Suvoda, have combined their offerings into a powerful streamlined integration with the convenience and simplicity of a single solution, without sacrificing the advanced functionality of standalone systems. This integration accommodates advanced study designs while driving down build and casebook complexity.

Hear directly from the sponsor, Cara Therapeutics, on the benefits they’ve seen in their studies by moving from a single provider to a harmonized, best-of-breed approach. The discussion will also include other examples illustrating how both companies support patient cohort branching, treatment cycles and system integrations.

Join this free webinar to learn about: 

• How a harmonized IRT & EDC integration can transform clinical trial execution
• The benefits of utilizing two best-of-breed eClinical software solutions (pros and cons of the multi-vendor approach)
• How to optimize workflow and streamline patient randomization and drug supply management to support complex studies

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