Clinical trials should move at the speed of science

Unified workflow automation powering faster, higher-quality global drug development.

Proven Results

61% Faster Trial Execution on the FICS Platform

7 Months

First patient enrolled to drug marketing approval

Under 6 Weeks

50% of patients enrolled

Regulatory-Grade Data

Real-time, audit-ready data — no third-party conversion needed

Real-time monitoring

Zero reconciliation

Earlier safety signal detection

Faster database lock

Phase II immuno-oncology trial for a global public biotech on FICS platform

Milestone	Traditional CRO & Stack	Pi Health + FICS
Study Conduct Duration Study start to last subject enrolled	13 months	6.5 months
Study Close-out Duration LSLV to DBL	5.5 months	2 weeks
Time to Clinical Report DBL to TFL	2 months	2 weeks
Total	20.5 months	8 months

The Evolution

The Evolution of Clinical Trial Technology

Each generation reduces operational friction — FICS eliminates it.

Capability	Gen 1: Legacy Stacks	Gen 2: Integrated Platforms	Gen 3: AI-Driven Clinical Trial Operating Systems FICS OS
Unified clinical data layer
Workflow-driven trial execution
Real-time sponsor + site visibility
AI embedded in workflows
EMR → EDC automation
Automated validation (GxP)
Cross-system data reconciliation	Manual reconciliation required	Partially reduced	Eliminated

Case Study

FICS Accelerates Feasibility and Site Selection

Reduced feasibility timelines by ~1 month in phase II global study for a top 10 pharma company.

40+

Sites completed feasibility questionnaires in FICS

37 Days

Earlier site responses than average

Seconds

For fully automated TMF filing

What Our Partners Say

Trusted by Industry Leaders

“We are using so many systems that are not talking to each other... I really like what Pi has built. It will help clinical sites. We do too much checking, rechecking, asking questions, if it’s good from the beginning, we don’t have to spend that much time.”
Global Head of Clinical Operations(Leading biotech)

In the News