From emerging biotech to global CROs. Every tier includes ICH E6(R3) §5.18 compliance checks, EDC integration, and AI-generated report narratives.
All data is encrypted at rest (AES-256) and in transit (TLS 1.3). We are SOC 2 Type II certification in progress. Data residency in US or EU is available on Enterprise plans. We do not use customer trial data to train models. A full security questionnaire is available on request.
SOC 2 Type II audit is underway — report available to Enterprise customers under NDA. Artha supports 21 CFR Part 11 requirements including audit trails, electronic signatures, and access controls on Enterprise plans. We can provide a validation package (IQ/OQ/PQ documentation) to support your computer system validation process.
Starter and Professional customers are typically live within 1–2 weeks. EDC integration setup (Medidata, Veeva) adds 3–5 business days. Enterprise deployments with custom integrations range from 3–6 weeks. We provide dedicated onboarding support and can work with your IT and validation teams throughout the process.
Yes. We offer a structured pilot program — typically 4–8 weeks on a subset of your active trials. This includes full feature access, onboarding support, and a side-by-side comparison against your current process. Pilots are available for Professional and Enterprise tiers. Request a demo to discuss terms.
Professional includes native integrations with Medidata Rave and Veeva Vault. Enterprise adds Oracle Clinical and Parexel Inform, plus API access for proprietary or custom EDC systems. All integrations are read-only — Artha pulls data to generate reports and does not write back to your EDC.
Annual contracts lock in your rate for the full contract term. Month-to-month pricing is available at a 15% premium. Enterprise contracts include price stability provisions. We provide 90 days advance notice of any pricing changes at renewal. Multi-year agreements with additional discounts are available for Enterprise customers.