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Enterprise InfrastructureInstitutional-Grade

The AI Infrastructure Layer for Institutional Biotech.

Palantir-grade infrastructure logic. NVIDIA-style architecture messaging. Built for pharma enterprises, CROs, academic medical centers, and government health agencies that require institutional security, regulatory alignment, and scientific precision — not SaaS features.

HIPAA-ReadyGDPR-AlignedGxP-AwareFDA 21 CFRICH E6(R2)SOC 2 Roadmap
400+
Organizations Deployed
99.9%
Uptime SLA
$5M+
Largest Contract Value
<4hr
Enterprise SLA Response
Institutional Positioning
Palantir-Grade
Infrastructure Logic
NVIDIA-Class
Architecture Model
Institutional
Procurement Ready
Institutional Deployment Models

Built for Every Institutional Structure

Five deployment architectures — each designed for the unique procurement, compliance, and operational requirements of its institutional category.

Large Cap / Mid Pharma

Pharma Enterprise Licensing

Multi-site deployment with dedicated AI infrastructure, white-label configuration, and integrated Veeva/Salesforce data flows. Covers all commercialization functions from IND to post-approval market access.

Dedicated compute cluster
Veeva CRM native integration
Multi-jurisdiction compliance
Custom model fine-tuning
Contract Research Organizations

CRO Infrastructure Partnerships

Infrastructure licensing that CROs deploy as a billable service layer for their biotech clients — enabling AI-assisted trial intelligence, site selection optimization, and automated scientific reporting.

CRO white-label deployment
Per-client data isolation
GCP-compliant workflows
API reseller access
NIH / CDC / BARDA / NHS

Government & Public Health Deployment

Sovereign cloud-compatible deployment for government health agencies and defense biomedical programs. FedRAMP-aligned architecture with full data residency controls and classified-compatible integration pathways.

Sovereign cloud support
FedRAMP-aligned architecture
On-premise deployment option
Inter-agency data protocols
Health Systems / Academic Medical Centers

Clinical AI Infrastructure Integration

Embedded AI layer for clinical research units at academic medical centers and health systems — connecting trial intelligence, biomarker analysis, and regulatory documentation pipelines to existing EHR infrastructure.

HL7 FHIR integration
EHR-compatible data ingestion
IRB-compliant audit trails
Clinical research automation
Air-Gapped / High-Security

Private Scientific Cloud Deployment

Fully isolated private cloud deployment for organizations with stringent data sovereignty requirements — biodefense contractors, rare disease companies handling sensitive patient cohorts, or Phase I trial units.

Air-gap compatible
Zero external data transfer
On-premise GPU compute
Custom security audit support

Custom Deployment Architecture

Don't see your institutional model? Our solutions team designs custom deployment architectures for unique organizational structures.

Deal Structures

Institutional Engagement Models

Three deal structures designed for different organizational maturity levels and infrastructure investment horizons.

Mid-Market Deployment
$500K – $2M
12-month contract
Most Common

Full-platform deployment across multiple product lines or regions. Includes all five infrastructure layers, dedicated compliance configuration, custom model training, and quarterly infrastructure reviews.

Ideal For

Late-stage biotechs, emerging pharma, large CROs

What's Included
Full 5-layer stack deployment
Multi-region optimization
Custom model fine-tuning
Dedicated CSM + engineering
Quarterly architecture reviews
Typical Timeline
Scoping
Deployment
Optimization
Scale
Enterprise Trust Architecture

Security Built for Institutional Procurement

Every security and compliance capability is designed to pass enterprise procurement reviews, institutional security audits, and regulatory due diligence processes out of the box.

HIPAAActive

Business Associate Agreement available

GDPR Art.6Active

EU/EEA data residency controls

SOC 2 Type IIIn Progress

Audit in progress — Q3 2026

GxP WorkflowsActive

GCP, GMP, GLP alignment

FDA 21 CFR Part 11Active

Electronic records & signatures

ICH E6(R2)Active

GCP trial documentation standards

AES-256 EncryptionActive

At-rest and in-transit

RBAC & SSOActive

SAML 2.0 / OIDC / Okta / Azure AD

Tenant IsolationActive

Zero cross-tenant data access

End-to-End Encryption

AES-256 at rest, TLS 1.3 in transit, zero-trust network architecture. No plaintext data at any layer of the stack.

Tenant Data Isolation

Complete logical and physical isolation between tenants. No shared storage, no cross-tenant queries, no shared inference context.

Immutable Audit Infrastructure

Cryptographically signed, append-only audit logs. Every AI decision, user action, and data access event recorded and tamper-proof.

Enterprise Case Studies

Institutional Deployment Evidence

Four documented enterprise deployments across pharma, genomics, CRO, and clinical research — with full infrastructure context, regulatory impact, and measurable outcomes.

Translational Oncology

NovaTera Biosciences

Boston, MA · Phase II/III

Challenge

A precision oncology company with three concurrent Phase II trials was spending 14 weeks per cycle manually synthesizing clinical data, generating investor updates, and managing regulatory documentation across FDA and EMA jurisdictions simultaneously.

Infrastructure Deployed
AI Scientific Intelligence LayerRegulatory & Compliance InfrastructureData & Computational Infrastructure
Scientific Workflow Accelerated

Translational analysis pipelines ingested raw Phase II efficacy data from three trial sites, cross-referenced against biomarker signatures, and generated investor-grade interim analysis narratives automatically.

Regulatory Impact

CIPHER engine configured for dual-jurisdiction (FDA/EMA) review. All 47 interim reports passed regulatory pre-screening without manual revision.

Translational Oncology
Operational Outcomes
14 weeks → 72hrs
Pipeline Cycle Time
$3.1M
Operational Cost Savings
100%
Regulatory Pre-Screen Pass Rate
2.4×
Investor Meeting Conversion Rate

Enterprise Infrastructure Capabilities

Every enterprise capability is designed to meet institutional procurement standards — not consumer product requirements.

Dedicated Compute Clusters

Isolated tenant infrastructure with guaranteed resource allocation and SLA-backed uptime.

Custom Model Fine-Tuning

Domain-specific model training on your proprietary scientific data and therapeutic area.

White-Label Deployment

Full brand customization — domain, UI, email templates, and reporting formats.

SSO / SAML 2.0 / OIDC

Enterprise identity management via Okta, Azure AD, Ping Identity, or any SAML 2.0 provider.

Role-Based Access Control

Granular permissions by department, geography, therapeutic area, and data sensitivity level.

Full API + GraphQL Access

Build custom internal tools and integration pipelines on top of the AI commercialization engine.

Data Residency Controls

Choose EU, US, or APAC data centers. Air-gap and on-premise deployment available for sovereign requirements.

Dedicated Scientific CSM

Assigned Customer Success Manager with biotech domain expertise, weekly strategy reviews, and 4-hour engineering SLA.

Institutional Procurement

Start Your Enterprise Infrastructure Conversation.

Our enterprise solutions team scopes your exact deployment requirements, maps your regulatory environment, and delivers a custom infrastructure deployment proposal within 48 hours — no commitment required.