Clinical trial acceleration
AI agents screen patient registries against trial criteria, extract eligibility data from EHRs, and generate pre-screening reports. Reduce site identification time by 60%.
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Industries · Life Sciences
GxP-ready AI agents for clinical trials, regulatory submissions, pharmacovigilance, and R&D data orchestration.
AI agents screen patient registries against trial criteria, extract eligibility data from EHRs, and generate pre-screening reports. Reduce site identification time by 60%.
Automated compilation of eCTD sequences, Module 3 quality data, and CSRs. AI agents validate submission readiness, flag format inconsistencies, and track authority queries.
AI agents monitor literature, social media, and regulatory databases for adverse events. Automated ICSR case intake, duplicate detection, and narrative generation with MedDRA coding.
Multi-agent RAG pipelines across ELN, LIMS, and document repositories. AI agents synthesize research findings, generate hypothesis reports, and track experimental lineage.
21 CFR Part 11 compliant audit trails. Computer system validation (CSV) with GAMP 5-aligned documentation. Role-based access, e-signatures, and tamper-proof logs.