Compliance & Validation — Not documented by Atlas
Ask the vendor: Which compliance certifications (HIPAA, 21 CFR Part 11, SOC 2, GxP) do you hold?
YPrime
eClinical technology company providing eCOA and IRT platforms for clinical trials.
YPrime, headquartered in Malvern, Pennsylvania, provides electronic clinical outcome assessment (eCOA) and interactive response technology (IRT/RTSM) platforms for clinical trials, competing with the established eCOA/IRT vendors. The company has been adding AI-assisted capabilities around study build and data review. As with any eCOA/IRT provider, per-study validation documentation and instrument licensing should be reviewed for regulated use.
- Headquarters
- Malvern, United States
- Deployment options
- cloud
- Website
- https://yprime.com
- https://www.linkedin.com/company/y-prime
Categories
AI Use Cases
- Digital/Decentralized Trials
Vendor Scorecard
50% — Partial coverage. Coverage score — how completely Atlas documents YPrime across 7 buyer-evaluation areas. Reflects available Atlas data, not solution quality.
Deployment & Hosting — Documented
cloud
Pricing Transparency — Not documented by Atlas
Ask the vendor: What is your pricing model, and what drives total cost of ownership?
Implementation & Onboarding — Not documented by Atlas
Ask the vendor: What is a realistic implementation timeline, and what onboarding support is included?
Organization & Role Fit — Documented
Mid-Size Biotech, Large Pharma, CRO / CDMO, Clinical Operations, Data Management
Solution Scope — Documented
Clinical Data Management
Company Viability — Partially documented
Private
Always ask the vendor
Not captured in Atlas data — confirm directly. Excluded from the score above.
Data Rights & IP
Who owns model outputs? Is our proprietary data used to train models others can access, and where does our data reside?
Model Credibility & Explainability
Can you share validation studies or benchmarks, explain how the model reaches its conclusions, and describe how bias and drift are monitored?
Questions to Ask This Vendor
- What does the study build timeline look like for our protocol complexity?
- Which AI-assisted features are in production, and what do they automate?
- What validation and compliance documentation is provided per study?
- How is instrument licensing and translation handled for our endpoints?