Expert pharma technology consulting for pharmaceutical companies, biotech firms, and CROs. FDA-compliant software development, clinical trial management systems (CTMS), drug discovery informatics platforms, pharmacovigilance systems, and regulatory reporting tools that accelerate drug development and ensure GxP compliance.
From FDA validation requirements to clinical data complexity, we help pharma companies build compliant, scalable systems — accelerating clinical trials, automating regulatory submissions, and enabling drug discovery innovation while maintaining GxP and 21 CFR Part 11 compliance.
Full-stack pharma tech: clinical trial management systems (CTMS), electronic data capture (EDC), drug discovery informatics, pharmacovigilance (PV) systems, regulatory submission tools (eCTD), laboratory information management systems (LIMS), and GxP-validated software development.
FDA 21 CFR Part 11 validation. GxP compliance built in. Audit-ready systems.
End-to-end trial management. Patient recruitment. Data collection. Real-time monitoring.
ML-powered compound screening. Predictive models. Accelerate research timelines.
It helps life-sciences organizations digitize R&D, clinical, manufacturing, and commercial operations with validated, compliant systems and data and AI platforms that accelerate discovery and time to market.
We build and document systems to GxP expectations with computer-system validation, traceability, and audit readiness, so quality and regulatory teams can rely on them.
Yes. We unify clinical, lab, and real-world data into governed platforms and apply AI for signal detection, trial optimization, and faster insight.
AI accelerates drug discovery, optimizes trials, improves pharmacovigilance, and streamlines manufacturing quality, all within validated, auditable guardrails.
Pharmaceutical and biotech companies, CROs, and life-sciences platforms modernizing data, cloud, and AI under strict compliance.
Partner with iAastha for pharmaceutical technology consulting — FDA-compliant software development, clinical trial systems, regulatory reporting, pharmacovigilance, and drug discovery platforms. Let’s build pharma technology that speeds innovation without compromising compliance.