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Simple, Transparent Pricing

Pay per study, per month. No per-user fees. More trials, more savings.

Starter

£999 /study/month

or £799/mo billed annually

For emerging biotech and academic research teams

  • 1 study per subscription
  • Up to 10 sites per study
  • 5 GB secure document storage
  • All core EDC features
  • Edit checks & auto-queries
  • E-signatures (Part 11 compliant)
  • Data export (CSV, ODM)
  • Email support (24h response)
Most Popular

Professional

£1,499 /study/month

or £1,199/mo billed annually

For growing research organizations running multiple trials

  • Everything in Starter, plus:
  • Unlimited sites per study
  • 50 GB secure document storage
  • Full AI suite (Protocol-to-eCRF, Auto-coding, Anomaly Detection)
  • SDTM export & CDISC mapping
  • Advanced randomization engine
  • Risk-based monitoring dashboard
  • Priority support (4h response)
  • Dedicated customer success manager

Enterprise

Custom /study/month

For CROs and large pharmaceutical organizations

  • Everything in Professional, plus:
  • Dedicated single-tenant infrastructure
  • Custom SSO (SAML 2.0, Azure AD, Okta)
  • SOC 2 Type II readiness and compliance documentation
  • IQ/OQ/PQ validation support
  • 99.9% SLA uptime guarantee
  • On-premise deployment option
  • Custom integrations (CTMS, eTMF, RTSM)
  • White-label option

Full Feature Comparison

Every plan includes core EDC compliance features. See what is included at each tier.

Feature Starter Professional Enterprise
Active Studies Up to 3 Unlimited Unlimited
Sites Up to 10 Unlimited Unlimited
Users Unlimited Unlimited Unlimited
Document Storage 5 GB 50 GB Custom
No-Code eCRF Builder
Visit Schedule Engine
E-Signatures (Part 11)
Immutable Audit Trails
Query Management
Edit Checks & Auto-Queries
Adverse Event Capture
Lab Data Management
Data Export (CSV, ODM)
SDTM Export & CDISC Mapping
AI Suite (Protocol-to-eCRF, Auto-Coding)
Anomaly Detection
Risk-Based Monitoring Dashboard
Advanced Randomization
SSO (SAML 2.0 / Azure AD / Okta)
Dedicated Infrastructure
On-Premise Deployment
IQ/OQ/PQ Validation Support
SOC 2 Type II Readiness Documentation
Custom Integrations
White-Label Option
SLA Uptime Guarantee 99.5% 99.9% 99.9%
Support Response Time 24 hours 4 hours 1 hour
Customer Success Manager

Pricing Questions

Common questions about pricing, billing, and plans.

Yes. Every plan includes a 14-day free trial with full access to all features. No credit card required to start. At the end of the trial, choose a plan or export your data.

Yes, you can upgrade or downgrade your plan at any time. Upgrades take effect immediately and are prorated. Downgrades take effect at the end of your current billing cycle. You can also switch between monthly and annual billing.

Your data is always preserved. If you downgrade to a plan with lower study or site limits, existing studies remain accessible in read-only mode. You can export all data at any time in CDISC ODM, CSV, or JSON format. No data is ever deleted without your explicit request.

Yes. We offer a 50% discount on Starter and Professional plans for verified academic and non-profit research institutions. Contact our sales team at sales@pharmatrialscortex.com with your institutional email for verification.

No per-user fees, ever. You pay per study, per month — the more studies you run, the lower your per-study cost. The Starter tier supports one study with up to 10 sites. Professional and Enterprise tiers offer volume discounts for organizations running multiple trials simultaneously.

We accept all major credit cards (Visa, Mastercard, American Express) and bank transfers for annual plans. Enterprise customers can pay via purchase order with net-30 terms. All prices are in GBP.

Annual billing provides a 20% discount compared to monthly pricing. You are billed once per year for the full amount. Annual plans can be cancelled at any time, with the remainder of the prepaid term still available.

Not Sure Which Plan Is Right?

Talk to our team. We will help you find the right plan based on your trial portfolio, team size, and compliance requirements.