Agent authors.
Human approves.
Inspection passes.





Day-0 compliance ships with every release.

Klariflow is the AI-native Paperless Validation System for pharma and biotech. Your validation pack, drafted in days — not quarters. SMEs approve.

Launching end of June 2026

Three pillars. One platform.

Every decision in Klariflow is built around these three outcomes for life sciences teams.


Agent authors, human approves

AI agents draft your full validation pack — IQ, OQ, PQ — from your URS and SOPs. Your SMEs review and approve. The work is done; the decisions stay human.

AI agent authors validation pack, human SME approves

Validation in days, not quarters

Klariflow compresses months-long validation cycles into days. Protocol drafting, traceability, evidence collection — collapsed. Every release ships faster.


Validation compressed from quarters to days

Day-0 compliance, every release

21 CFR Part 11 audit trail on every agent action. Continuous validation that holds across releases. Complete, inspection-ready evidence from day one.

21 CFR Part 11 audit trail and inspection-ready compliance

Team

Decades of domain depth. Operator-grade software experience.


Abhinandan Sahgal

Abhinandan Sahgal

2× founder. 15 years building enterprise software. 3 patents. Scaled Tekion Corp to $150M ARR.

Venkat Kadiala

Venkat Kadiala

26 years in life sciences.

Vinay Parachuri

Vinay Parachuri

26 years in life sciences. Lived the validation problem firsthand.


52+ years in life sciences • 10 years operating a life sciences company

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