Biotech & pharma sponsors
Own your trial data end to end. DPDP Act 2023 aligned, with no vendor holding the master copy.
DPDP Act 2023 aligned consent and processing flows by default.
Submission-ready exports for CDSCO, and CDISC SDTM for international filings.
Export the full study, audit trail included, whenever you ask.
- 30 minutesTo see it running on your own protocolNo scoping call, no quote and no purchase order first.
- 10 minutesTo stand a study build up end to endThe eCRF itself is instant — the AI Designer drafts it from your protocol.
- No codeTo build your forms, checks and visit scheduleDoing it by hand takes most teams 4–8 weeks.
- OneData model behind every moduleEnter data once and it is everywhere. Nothing to match up later.
- ZeroExtra fees per form, per query or per exportThe 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.
Learn moreGeneric-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.
Learn moreMulti-therapy CROs
Phase II to IV across therapeutic areas, on one data model. Configurable workflows and a single continuous audit trail, whatever the indication.
Learn more