Solutions

Academic & government trial groups

Grant-funded research without enterprise-CRO overhead. Stand a study up on a research budget and keep the audit trail a regulator expects.

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Ethics-committee-aware workflows aligned to ICMR National Ethical Guidelines (2017).

Investigator-friendly capture for resident-led and registrar-led trials.

Pricing structured for grant-funded research, not commercial pharma budgets.

24 hours

To get a demo running on your own protocol

No scoping call, no quote and no purchase order first.

No code

To build your forms, checks and visit schedule

Doing it by hand takes most teams 4–8 weeks.

One

Data model behind every module

Enter data once and it is everywhere. Nothing to match up later.

Zero

Extra fees per form, per query or per export

The price is the same whether you collect 10 records or 10,000.

Other ways teams use Trialion

Bioequivalence (BA-BE) specialists

Replicate designs and intensive PK sampling, without a second system. Pre-built templates, volunteer randomization tied to dispensing, and ANDA-ready exports from the same data model.

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Generic-drug CROs

Short, focused trials, run at volume. Repeat protocol designs set up in days, priced per study or per month, with the whole portfolio on one data model.

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Multi-therapy CROs

Phase II to IV across therapeutic areas, on one data model. Configurable workflows and a single continuous audit trail, whatever the indication.

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