Solutions
Indian arms of global CROs
Sponsor-grade quality, DPDP-aligned, and CDSCO submission support — without disrupting the global team's tooling.
India-jurisdiction contracting.
Same audit trail and validation pack global sponsors expect from a Western EDC.
Integrations to SUGAM and CTRI so India-arm submissions don't bottleneck.
DPDP Act 2023
Aligned by design
Schedule Y
CDSCO-aligned by design
ISO 27001
Information security controls aligned
Other ways teams use Trialion
Bioequivalence (BA-BE) specialists
Built-in PK sampling schedules, replicate-design support, and ANDA-ready exports — for the segment where India leads global study volume.
Learn moreGeneric-drug CROs
Short, focused trials at scale — pricing and tooling aligned to how generic-drug development actually operates in India.
Learn moreMulti-therapy CROs
Phase II to IV across therapeutic areas — same data model, configurable workflows, one continuous audit trail.
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