Enterprise & Investor

Built for health systems.
Designed for scale.

Unified platform eliminates integration risk. One vendor replaces 6–7 disconnected systems β€” reducing procurement cycles by an estimated 8 months. Open standards, data portability guarantees, and modular architecture ensure zero vendor lock-in.

6β†’1
Vendors consolidated
8 mo
Procurement reduction
30 days
Live demo environment
MSKCC
Anchor client

The Problem We Solve

Clinical development is broken. These are the numbers that prove it β€” and the reason medinovAI exists.

$48K
Per-patient Phase III cost
Industry benchmark 2024
6.2 mo
Average site activation
vs. 2.8 mo with medinovAI
7.3
Systems per trial (avg)
Veeva 2023 CTMS Benchmark
340%
Regulatory cycle time inflation since 2018
FDA ESG analysis
42%
TMF inspection readiness at top-20 CROs
DIA TMF Reference Model
$2.1B
Annual clinical supply chain waste in oncology
IQVIA 2023
Revenue Architecture

Three Diversified Revenue Engines

Eliminating single-product concentration risk through vertical integration. Recurring enterprise subscriptions with multi-year commitments.

Enterprise Subscriptions

Recurring SaaS Revenue

Multi-year enterprise SaaS commitments. Land-and-expand: eTMF β†’ CTMS β†’ LIS β†’ EDC β†’ full platform. Each module adoption increases switching costs.

  • Multi-year MSAs
  • Land-and-expand model
  • 100% enterprise clients
Per-Visit Fees

Clinical Services Revenue

myOnsite per-visit clinical services under master service agreements. Protocol-bound visit volume commitments aligned to sponsor enrollment projections.

  • Protocol-bound volumes
  • Forward revenue visibility
  • Zero consumer exposure
$
Per-Specimen Fees

Biospecimen Revenue

ICMR-licensed, FDA-authorized procurement. Zero regulatory incidents. Premium pricing for compliance certainty. DescartesBio trans-sovereign pipeline.

  • ICMR-licensed
  • FDA-authorized
  • Premium compliance pricing
Singular Global Market Position

Structural Competitive Moats

Advantages that cannot be replicated by any single competitor in the market.

Only entity with simultaneous first-party ownership of IND-authorized DCT phlebotomy + AI-native clinical SaaS + ICMR-licensed biospecimen procurement + direct FDA ESG eCTD submission

MSKCC β€” #1 NCI-designated oncology institution β€” selected myOnsite as IND-authorized decentralized phlebotomy provider

DescartesBio 15,000+ clinically-annotated oncology specimens representing South Asian genomic architectures absent from all major Western biobank reference populations

Vertical integration collapses 7 independent MSAs, SOC 2 attestation reviews, and BAA negotiations into a single contractual framework

Cryptographic hash chain provenance β€” mathematically verifiable proof from needle to NDA β€” no competitor can replicate

Deal Flow

From Discovery to Strategic Partnership

Reducing 18-month vendor cycles to accelerated value delivery.

01

Discovery

AI-personalized presentation adapts in real-time to your role, interests, and organization β€” eliminating generic sales decks.

02

Qualification

Tiered access levels reveal progressively deeper intelligence β€” from public overview through NDA-protected documentation.

03

Proof of Value

Pre-configured environment demonstrates full capabilities within 30 days β€” de-risking the commitment decision with real trial data.

04

Land & Expand

Start with eTMF, add CTMS, then LIS and EDC β€” each module shares the same data, auth, and audit infrastructure.

Investor Portal

Access the Full Investment Thesis

The full 28-slide presentation β€” including platform architecture deep-dive, revenue model, competitive analysis, team, and financial projections β€” is available to qualified investors and strategic partners. Access is currently available to US-based organizations.

Equity or strategic investment
Clinical trial sponsor or site
Health system or payer partnership