Simple pricing.Predictable margins.
From single bioequivalence studies to multi-site CRO portfolios.
A single active study on the live Trialion EDC, with supported integrations to your existing CTMS, eTMF, eConsent, ePRO, RTSM, safety, and coding tools. Suited to individual bioequivalence studies and Phase II pilots.
- Modern EDC live in India, CDSCO Schedule Y aligned
- Up to 5 active sites
- Pre-built BA-BE templates included
- Supported integrations: CTMS, eTMF, RTSM, eConsent, ePRO, safety, coding
- CDSCO submission packs + CDISC SDTM-aligned exports
- Email support and standard validation pack
A multi-site portfolio across concurrent studies. EDC live now; native modules ship onto the same data model as released — without a migration project. Suited to mid-size Indian CROs and the Indian operations of global CROs.
- Multiple concurrent studies
- Unlimited active sites across India
- Native modules as they ship (CTRI/CTMS and eTMF next)
- Roadmap influence and early access to in-build modules
- DPDP Act 2023 aligned, with optional regional failover
- Priority support and dedicated CSM in IST
Large Indian CROs, Indian operations of global CROs, and pharma sponsors requiring dedicated environments, custom SLAs, and a named architect on the account.
- Unlimited studies, multi-tenant role engine
- Dedicated single-tenant environments
- Custom SLAs and uptime guarantees
- Full validation packs and Indian-GCP audit support
- 24/7 support, named architect, named product partner
See what Trialion saves you.
Model the manual data-management hours auto-validation gives back to your team — and the plan that fits.
Tell us about your study
Model the hours and dollars Trialion gives back across data management, site monitoring, and the program as a whole.
Average queries raised per page before automation kicks in.
Share of manual queries eliminated by auto-validation.
Modeled on the live Trialion EDC. CRA savings include remote SDV against integrated source systems and reduced tier-2/3 site travel. As native modules ship onto the same data model, additional savings compound automatically — no rebuild, no re-platforming. GST applied on top of subscription fees.
Hours saved on manual validation & query resolution.
Remote SDV and targeted site visits via continuous monitoring.
~20% faster to database lock.
Net of the Trialion subscription on the Launch tier. Book a demo for a quote.
A single active study — BA-BE or pilot Phase II — on the live Trialion EDC with integrations to the rest of the eClinical stack.
Frequently asked
What ships in v1?+
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/SUGAM integration), eTMF, eConsent, ePRO, RTSM, safety, and coding are delivered through supported integrations until each native module is released.
How is Trialion India 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 the validation pack 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 operates on controls aligned to ISO 27001, ISO 27017, and ISO 27018. 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 via the SUGAM portal 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 the roadmap?+
CTMS (with CTRI/SUGAM 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 Octalsoft, Castor India, MaxisIT, or paper?+
Yes. Our migration team has standard playbooks for the principal Indian EDCs and paper or Excel data rooms. Typical migration is 4–6 weeks and generally proceeds without pausing site activity.