We deliver audit-ready smart contracts in 2-4 weeks, from initial concept to mainnet deployment. Our process is built on battle-tested patterns and security-first development.
LABS
Services
Clinical Trial Data Tokenization
We develop secure blockchain systems to tokenize clinical trial datasets as NFTs or fungible tokens. Enable compliant data licensing, maintain immutable provenance, and unlock new revenue for research consortia.
Chainscore © 2026
overview
CORE SERVICE
Smart Contract Development
Secure, production-ready smart contracts built for speed and reliability.
Reduce your time-to-market and technical risk with contracts that just work.
- Expertise in:
Solidity0.8+,Rust(Solana/Sealevel),Vyper, andCairo(Starknet). - Security Foundation: Built with
OpenZeppelinlibraries and internal security checklists. - Full Lifecycle: Development, unit/integration testing, deployment scripting, and post-launch monitoring.
key-features-cards
ENTERPRISE-GRADE INFRASTRUCTURE
Core Capabilities of Our Tokenization Platform
Our platform provides the technical foundation to tokenize clinical trial data with institutional-grade security, regulatory compliance, and seamless integration into your existing workflows.
01
Regulatory-Compliant Smart Contracts
Custom-built tokenization logic (ERC-3643, ERC-1155) with embedded KYC/AML checks, investor whitelisting, and automated compliance rules for clinical data access.
100%
Audit Coverage
OpenZeppelin
Security Standard
02
HIPAA & GDPR-Aligned Data Vaults
Secure, permissioned off-chain storage for sensitive PHI and trial data. Data is encrypted, hash-anchored to the blockchain, and access is gated by on-chain token ownership.
AES-256
Encryption
Zero-Knowledge
Proofs Supported
03
Granular Access & Monetization
Implement fine-grained, time-bound data access tiers. Enable direct micropayments for dataset queries, model training, or result verification, automating revenue distribution to data contributors.
Sub-second
Access Grants
< $0.01
Tx Cost
04
Provenance & Audit Trail
Immutable, timestamped ledger of all data contributions, access events, and consent updates. Provides an irrefutable audit trail for regulators, sponsors, and ethics boards.
Immutable
Record
Real-time
Tracking
05
Interoperable Data Oracles
Secure bridges to ingest and verify real-world data from EDC systems, EHRs, and IoT devices. Bring off-chain clinical events on-chain to trigger smart contract logic.
99.9%
Uptime SLA
Chainlink
Oracle Network
06
White-Label Participant Portal
Branded web interface for trial participants to manage consent, view tokenized rewards, and control their anonymized data sharing preferences with full transparency.
< 2 weeks
Deployment
Mobile-First
Design
benefits
MEASURABLE IMPACT
Business Outcomes for Your Research Consortium
Move beyond proof-of-concept to a production-ready data ecosystem that delivers tangible value to all stakeholders, from sponsors to patients.
01
Accelerated Trial Timelines
Reduce data reconciliation cycles from weeks to minutes with automated, auditable data pipelines. Our tokenized framework ensures real-time access to clean, standardized datasets for faster analysis and decision-making.
Up to 90%
Faster Data Reconciliation
Real-time
Site Data Access
02
Enhanced Data Integrity & Auditability
Immutable, timestamped audit trail for all data submissions and protocol amendments. Built-in compliance with FDA 21 CFR Part 11, ALCOA+ principles, and GDPR via zero-knowledge proofs for patient privacy.
Immutable
Audit Trail
ALCOA+
Compliance Built-in
03
Reduced Operational Friction & Cost
Eliminate manual data aggregation and costly intermediary platforms. Smart contracts automate participant incentives, site payments, and data validation, slashing administrative overhead.
> 40%
Lower Admin Costs
Automated
Incentive Payouts
04
New Monetization & Collaboration Models
Securely license tokenized, anonymized datasets to academic institutions or pharma partners. Create transparent revenue-sharing models with contributing research sites using programmable smart contracts.
New Revenue Streams
From Legacy Data
Transparent
Revenue Sharing
05
Increased Participant Engagement & Retention
Implement direct, verifiable reward mechanisms for patient-reported outcomes. Provide patients with sovereign control and visibility over their contribution, fostering trust and long-term study adherence.
Improved
PRO Compliance
Patient-Centric
Data Control
06
Future-Proof Interoperability
Designed for the decentralized science (DeSci) ecosystem. Our architecture ensures seamless integration with emerging tools for computational biology, AI analysis, and cross-institutional data lakes.
DeSci-Ready
Architecture
Standardized
Data Schemas
Risk-Mitigated Deployment Roadmap
Phased Implementation for Controlled Scaling
A structured, milestone-driven approach to tokenizing clinical trial data, designed to de-risk the process and demonstrate value at each stage before full-scale investment.
| Implementation Phase | Core Deliverables | Timeline | Investment | Key Outcome |
|---|---|---|---|---|
Phase 1: Proof of Concept | On-chain data schema design Pilot smart contract (ERC-721/1155) Basic dashboard for 1 trial site | 2-4 weeks | $15K - $25K | Technical feasibility proven Stakeholder buy-in secured |
Phase 2: Pilot Deployment | Full tokenization logic for 1 trial Regulatory compliance review Participant consent & data ingress API Audited smart contracts | 6-8 weeks | $50K - $80K | Live, compliant data flow Real-world validation with users |
Phase 3: Multi-Trial Scaling | Multi-tenant architecture Advanced analytics & reporting module Integration with EDC/ePRO systems Full security audit & penetration test | 8-12 weeks | $120K - $200K | Platform ready for enterprise rollout Operational efficiency gains realized |
Ongoing: Enterprise Support | 24/7 platform monitoring & incident response Smart contract upgrade management Quarterly security reviews SLA: 99.9% uptime, 4h response | Ongoing | Custom (Annual Retainer) | Guaranteed reliability Continuous compliance & innovation |
how-we-deliver
COMPLIANCE BY DESIGN
Our Methodology for Regulated Environments
We build clinical trial data tokenization platforms with regulatory compliance as a core architectural principle, not an afterthought. Our methodology ensures your solution meets HIPAA, GDPR, and 21 CFR Part 11 requirements from day one.
01
Regulatory-First Architecture
We design tokenization logic and data flows around immutable compliance rules. Smart contracts enforce patient consent management, data access controls, and audit trails, creating a verifiable chain of custody for regulatory audits.
HIPAA/GDPR
Architected For
21 CFR Part 11
Compliance
02
Privacy-Preserving Data Layers
Implement zero-knowledge proofs (ZKPs) and secure multi-party computation (sMPC) to enable data analysis and proof-of-concept validation without exposing raw patient data. Keep sensitive PHI off-chain while proving data integrity on-chain.
ZK-Proofs
Privacy Tech
PHI Off-Chain
Core Principle
03
Role-Based Access Control (RBAC)
Granular, on-chain permissioning for sponsors, CROs, sites, and regulators. Define immutable access policies for data viewing, contribution, and audit functions, with all actions cryptographically logged for compliance reporting.
Granular Roles
Permission Model
Immutable Logs
Audit Trail
04
End-to-End Audit Trail
Every data point submission, consent update, and access request is immutably recorded on a permissioned ledger. Generate regulator-ready reports instantly, providing tamper-proof evidence of protocol adherence and data handling.
Tamper-Proof
Record Keeping
Instant Reports
For Audits
06
Interoperability & Data Portability
Build with standards like HL7 FHIR and W3C Verifiable Credentials in mind. Our systems are designed for seamless, compliant data exchange with existing EDC systems, EHRs, and future regulatory data warehouses.
HL7 FHIR
Data Standard
W3C VCs
Credential Standard
security-compliance
FOUNDATION
Custom Blockchain Development
Build a purpose-built blockchain or L2 tailored to your specific use case and performance requirements.
We architect and implement bespoke blockchain networks and Layer 2 solutions from the ground up. Our approach moves beyond generic frameworks to deliver a chain optimized for your unique needs in throughput, finality, and governance.
A custom chain is not a luxury—it's a strategic asset for applications requiring unmatched performance, control, or specialized functionality.
- Substrate & Cosmos SDK: Development on leading modular frameworks for sovereign app-chains.
- Optimistic & ZK Rollups: Custom L2s on Ethereum for scalability with inherited security.
- Consensus & VM Design: Tailor consensus mechanisms and virtual machines for your transaction profile.
- Bridge & Interop Architecture: Secure, trust-minimized bridges to connect your ecosystem.
- Full Node Infrastructure: Deployment and management of your network's foundational nodes.
For CTOs and Data Architects
Clinical Data Tokenization: Key Questions
Technical and operational details for leaders evaluating blockchain solutions for clinical trial data.
Standard clinical data tokenization platforms deploy in 4-6 weeks from kickoff to production. This includes requirements analysis, smart contract development, on-chain integration, and a full security audit. Complex multi-study or cross-chain implementations may extend to 8-10 weeks.
ENQUIRY
Get In Touch
today.
Our experts will offer a free quote and a 30min call to discuss your project.
NDA Protected
Confidentiality24h Response
Time to ValueDirectly to Engineering Team
No Sales Fluff10+
Protocols Shipped
$20M+
TVL Overall