The rise of clinical trial complexity and global studies means your IRT technology needs to be capable of heavy lifting, so you can focus on clinical study execution. YPrime’s full-service end-to-end IRT systems help clinical teams and clinical supply professionals do more with less.
Our technology solutions and domain expertise ensure statistical integrity upfront, reduce risk during your trial and delivery submission-ready data at the end of every project
- Pre-study: YPrime’s statistical experts generate randomization and material lists for IRT systems
- During study: YPrime project managers bring in-depth experience of best practices and common pitfalls to provide design recommendations, manage scope, as well as communicate and mitigate risk early to keep your study on track
- Post-study: Knowledge of CDISC delivers submission-ready deliverable to eliminate costly and time-intensive data transformation
Rely on YPrime’s technology for:
- Self-Service Tools and Clinical Supply Management
- Ability to support post-go live functionality
- A range of solutions, from out of the box simplified Phase I to full-featured systems capable of supporting global Phase III studies
- Flexible enough to support dynamic dispensation management needs of a clinical trial
- Ability to support complex study designs – from one of a kind to first of a kind
- Comprehensive configuration library to support a range of scenarios, with ability to customize as needed. Clients can expect a solution that is 90% configurable
Minimize your clinical trial risk with YPrime’s IRT solutions.
USA, UK, Macedonia, Australia, China