Solutions
Academic & government trial groups
Designed for AIIMS-equivalent, ICMR-funded, and DBT-funded research — without enterprise-CRO overhead or USD pricing.
Ethics-committee-aware workflows aligned to ICMR National Ethical Guidelines (2017).
Investigator-friendly capture flows for resident-led trials.
Pricing structured for grant-funded research, not commercial pharma budgets.
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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