Solutions

Biotech & pharma sponsors

Own your trial data, end to end — under DPDP Act 2023, with in-jurisdiction contracting.

Aligned to the DPDP Act 2023 by default.

DPDP-compliant consent and processing flows.

Submission-ready exports for CDSCO, and CDISC SDTM for international filings.

DPDP Act 2023

Aligned by design

Schedule Y

CDSCO-aligned by design

Audit trail

Continuous, immutable, inspection-ready

Other ways teams use Trialion

Built-in PK sampling schedules, replicate-design support, and ANDA-ready exports — for the segment where India leads global study volume.

Short, focused trials at scale — pricing and tooling aligned to how generic-drug development actually operates in India.

Phase II to IV across therapeutic areas — same data model, configurable workflows, one continuous audit trail.