In the dynamic landscape of clinical trials, where time is of the essence, having the right Interactive Response Technology (IRT) partner significantly impacts study timelines. At YPrime, we demonstrated unparalleled efficiency for a top pharma partner, resulting in faster startup times with the ability to implement protocol amendments quickly and seamlessly. 

For this complex global study, we supported this top sponsor with:

Risk mitigation with pre-validated configurations

8x faster protocol amendment implementation

And customer service support

At YPrime, we pioneer solutions that streamline the clinical trial journey, increasing certainty from study design to data lock. Download this case study and find out why top pharma leaders and emerging biotech companies continue to choose YPrime for eConsent, eCOA, IRT, and patient engagement solutions.