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For Enterprise Pharma

Stop waiting on
service delivery.

Replace manual, months-long RWE workflows with evidence infrastructure that runs when you need it, across your entire portfolio.

Explore Capabilities
Evidence Generation Workspace
KOL INQUIRY / PROTOCOL

Calculate real-world overall survival (rwOS) for Asset X vs. Standard of Care in 2L+ metastatic NSCLC patients with EGFR mutations.

Frekil
Synthesizing 4.2M Records...Est: 0.8s
Publication-Ready ResultsREADY
Hazard Ratio
0.62
P-Value
< 0.001

The true cost of manual RWE.

Every time you ask a question, the clock starts. Months of data prep. Weeks of manual coding. An opaque process ending in a static report.

Frekil replaces manual workflows with scalable infrastructure. By standardizing OMOP mapping and enforcing rigorous protocols instantly, your team takes back control of timelines and quality — whether you run studies in-house or with partners.

Evidence Delivery Timelines
Traditional Process6-9 Months
Data Prep & Mapping
Manual Coding
QC & Reporting
Frekil AutomatedHours / Days
Automated Pipeline
*Assuming data access is already established. Bring Your Own Data (BYOD) instantly maps to OMOP.

Cross-Pipeline Intelligence

Unified evidence generation across multiple therapeutic areas. Standardize protocols and mappings universally.

Bring Your Own Data (BYOD)

We connect directly to your existing data lakes, EHR extracts, and licensed claims datasets. No need to migrate data.

High-Volume Scalability

Process millions of patient records simultaneously. Built for massive RWD/RWE pipelines without compromising speed.

Enterprise Security

Zero patient data exposure. Frekil executes within a secure, isolated sandbox. HIPAA and GDPR ready.

Ready to standardize?

Join the forward-thinking pharma organizations building their evidence infrastructure on Frekil.