Transform unstructured protocol synopses into ranked, encrypted site feasibility intelligence — in under 48 hours. Built on a zero-trust, HIPAA-compliant architecture.
Trusted by fast growing organizations worldwide
Process any document—including protocols, synopses, CSRs, SAPs, and PDFs—into structured, queryable intelligence.
Zero-Trust Architecture. Engineered for the stringent compliance requirements.
Run predictive models and coverage checks for protocol design and trial success.
Identify optimal trial sites based on historical performance.
Communicate directly with PIs, manage site relationships.
Deploy autonomous agents that continuously monitor regulatory shifts.
Automatically vectorize and link scattered clinical data into a unified semantic graph for high-precision AI retrieval.
Continuously synchronize with CMS, FDA, and global trial registries to provide baseline comparators and predictive metrics. Real-time connections keep your feasibility models up-to-date.
Continuous real-time synchronization with clinical registries and APIs.
Automated parsing of public protocols and historical trial outcomes.
Automated extraction of baseline metrics for accurate feasibility analytics.
No OpenAI. No Anthropic. No Google. We strictly deploy open-source intelligence locally within your isolated infrastructure. Your clinical trial protocols and proprietary data never leave the tenant environment.
Self-hosted LLMs ensuring no data leaves the environment.
Proprietary OCR and NLP pipelines isolated from external networks.
Absolute containment with no external vendor telemetry.
Deployed 100% within your own Virtual Private Cloud (VPC) and hardware. You retain absolute ownership over your clinical data. Neither we nor any third party have access to your environment—ensuring zero-trust data sovereignty.
Deployed directly onto your secure infrastructure for total isolation.
Seamless internal connectivity—data never leaves your firewall.
100% Client Data Ownership—we have zero access to your partition.
Connect natively to any major Electronic Data Capture (EDC) system. Our architecture is entirely vendor-agnostic, ensuring your clinical infrastructure remains flexible and free from vendor lock-in.
Pre-built connectors for industry-standard EDC platforms without tying you to a single provider.
Bi-directional synchronization ensures your central feasibility engine is always up to date.
Our platform operates entirely standalone by default. Integrate with specialized labs or public vendors only on an as-needed basis. Your proprietary data never leaves the tenant system unless explicitly routed.
By default, no data flows to external vendors. Establish highly-controlled, outbound-only bridges when required.
Bring in specialized external data without adopting proprietary formats. We normalize it securely inside your firewall.
Transform manual feasibility tracking into a deterministic, automated pipeline. Our orchestration engine wires complex routines—from multi-source ingestion to probabilistic risk scoring—directly into your clinical workflow.
Query protocol criteria using plain English, translated into secure SQL.
Model enrollment trajectories using historical FDA/CMS datasets.
Secure, cryptographically tied storage for IRBs and site contracts.
Automate repetitive site selection and feasibility assessment tasks.
Engineered for the stringent compliance requirements of modern pharmaceutical enterprises. Your data never leaves your isolated tenant partition, protected by multi-layered cryptographic enforcement.
Dedicated single-tenant schemas with AES-256 encryption at rest and TLS 1.3 in transit.
Immutable audit trails, forced re-authentication, and rigorous role-based access control.
Continuous monitoring and external validation of security and confidentiality principles.