A plan for every stage.
From a single bioequivalence study to a multi-site CRO portfolio. Quarterly subscriptions per trial — not sure which fits? Talk to us.
Every tier includes the whole mechanism. AI drafting, edit checks at the point of entry and the review-and-sign workflow are not a premium add-on — what changes between tiers is scale, not capability.
Plans
Launch
Available today- 1 active study
- Up to 5 sites
- Up to 10 users
- Email support, IST hours
Scale
- Up to 10 active studies
- Unlimited sites
- Up to 50 users
- Priority support + named CSM
Enterprise
- Unlimited studies
- Unlimited sites
- Unlimited users
- 24/7 support + named architect
Every feature, side by side.
Connectors and validation support are included on every tier, and so is the drafting and review workflow. No per-form, per-query, or per-export fees, and no capability held back for the tier above.
Scale Concurrent studies across a multi-site portfolio. Built for how a mid-size CRO actually runs. Book a demo | |||
|---|---|---|---|
| Study build & capture | |||
| eCRF designer with conditional logic | Included | Included | Included |
| Edit checks at the point of entry | Included | Included | Included |
| Pre-built BA-BE study templates | Included | Included | Included |
| Protocol amendments without a rebuild | Included | Included | Included |
| Mobile-first capture for low-connectivity sites | Included | Included | Included |
| Compliance & audit | |||
| Continuous audit trail | Included | Included | Included |
| Electronic signatures, freeze & lock | Included | Included | Included |
| CDSCO Schedule Y submission packs | Included | Included | Included |
| Validation support | Standard | Standard | Dedicated |
| Indian GCP audit support | Not included | Included | Included |
| Custom roles & permissions | Not included | Not included | Included |
| Data & integrations | |||
| CDISC SDTM-aligned exports | Included | Included | Included |
| CTMS, eTMF, RTSM, eConsent, ePRO, safety & coding | Included | Included | Included |
| CTRI registration support | Included | Included | Included |
| Central lab and hospital information system feeds | Not included | Included | Included |
| BI connectors (Power BI, Tableau) | Not included | Included | Included |
| Scheduled export & backups | Not included | Included | Included |
| Platform & support | |||
| Native modules as they ship, on the same data model | Included | Included | Included |
| Roadmap input and early access to in-build modules | Not included | Included | Included |
| Regional failover | Not included | Optional | Included |
| Dedicated single-tenant environment | Not included | Not included | Included |
| Custom SLAs and uptime guarantees | Not included | Not included | Included |
| Support | Priority + CSM | 24/7 + architect | |
Frequently asked
What's live today?+
The Trialion EDC — study build, eCRF capture, edit checks, queries, reports, CDSCO Schedule Y submission packs, CDISC SDTM-aligned exports, 21 CFR Part 11–style e-signatures, freeze, lock, and a continuous audit trail. CTMS (with CTRI integration), eTMF, eConsent, ePRO, RTSM, safety, and coding are delivered through supported integrations until each native module is released.
How is Trialion priced?+
Three tiers — Launch (single study), Scale (multi-site portfolio), and Enterprise (custom). No per-form, per-query, or per-export fees; integration connectors and validation support are included on every tier. Book a demo for a quote against your study design.
Where is the data hosted?+
Aligned to the DPDP Act 2023. The underlying cloud infrastructure encrypts data in transit and at rest, enforces role-based access, and logs every access for audit. Enterprise customers can opt in to regional failover or to a dedicated single-tenant environment; the full subprocessor list is published in our Data Processing Agreement.
Is the EDC aligned to CDSCO Schedule Y?+
Yes. Study templates, the audit trail, and electronic signatures are designed for Indian GCP and aligned to CDSCO New Drugs and Clinical Trials Rules, 2019. CTRI registration support is in build.
Does the EDC support BA-BE studies?+
Yes. Pre-built bioequivalence templates include replicate-design support, dosing-interval and PK sampling schedules, integrated volunteer-to-dispensing workflows, and ANDA-ready exports for international filings.
What's on the roadmap?+
CTMS (with CTRI integration) and eTMF are in build. eConsent, ePRO, RTSM, safety, and coding are sequenced on the published roadmap. Sequence may shift based on customer demand — Scale customers get input on prioritization.
What happens when native modules ship?+
Customers on the Launch and Scale tiers move from the integrated workflow to the native module on the same data model and audit trail, with no migration project. The data captured today is the data the new module operates on.
Can we migrate from our current EDC, or from paper?+
Yes. We have standard playbooks for commercial and self-hosted EDCs as well as paper and spreadsheet data rooms. Typical migration is 4–6 weeks and generally proceeds without pausing site activity.