Solving For Certainty—
De-Risking Clinical Trials from Study Design to Data Lock
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Clinical research is increasingly becoming more complex, making it challenging for trial sponsors to meet timelines, quickly implement system changes related to protocol amendments, and ultimately deliver high-quality data. Combining an agile, purpose-built process with the industry’s most sophisticated tech stack, YPrime’s technology platform can help you stay ahead.
With an average study start-up time of 31+ weeks and over 66% of clinical trials taking longer than planned, your technology must be seamless. From eConsent and IRT to eCOA and built-in patient engagement, our technology ecosystem allows you to focus on your next step. It’s intuitive enough for patients, and powerful enough for researchers.
YPrime has a proven history of de-risking clinical trials so you can move with certainty from study design to data lock. With 4x faster system changes related to protocol amendments (IRT) and up to 30% faster start-up times (eCOA), we’re here to support you.
View the latest insights by downloading our fact sheet here.