Operational Excellence Meets Regulatory Readiness
Streamline compliance, simplify submissions, and gain real-time clarity with Telperian’s tech-enabled services.
What is TES?
FDA Deliverables & Tech-Enabled Services (TES) is Telperian’s specialized offering for submission preparation, trial oversight, and real-time data review.
We bring automation, compliance, and biostatistical insight together to reduce reporting burdens and increase clarity.
Built for Submission and Oversight
TES works across your entire trial lifecycle—from live patient monitoring through FDA e-submissions. All tools are no-code, optimized for transparency, and integrate directly with your biostatistics and regulatory teams.
Design
Discussion
Design
Study
Study
Startup
Enrollment & Clinical
Follow-up
Analysis &
Reporting
TES Tools You Can Trust
Foundation Explore
Track trial-level trends with real-time dashboards for biomarkers, labs, vitals, and more.
Patient Landscapes
Get a scrollable, patient-specific overview with clinical outcomes, safety flags, and endpoint milestones.
TFL Generator
Automate creation of FDA-ready tables, figures, and listings—aligned with CDISC and regulatory submission standards.
Why Sponsors Use TES
Accelerate interim DMC and final submissions
Centralized patient-level and trial-wide views
Simplify safety monitoring with clear visualizations
Generate submission-ready TFL Generator with minimal manual work
Get FDA-Ready, Faster
