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Full-Stack Web3 dApp Development
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Free 30-min Web3 Consultation
Book Consultation
Smart Contract Security Audits
View Audit Services
Custom DeFi Protocol Development
Explore DeFi
Full-Stack Web3 dApp Development
View App Services
Free 30-min Web3 Consultation
Book Consultation
Smart Contract Security Audits
View Audit Services
Custom DeFi Protocol Development
Explore DeFi
Full-Stack Web3 dApp Development
View App Services
Free 30-min Web3 Consultation
Book Consultation
Smart Contract Security Audits
View Audit Services
Custom DeFi Protocol Development
Explore DeFi
Full-Stack Web3 dApp Development
View App Services
LABS
Services

Cross-Border Clinical Data Sharing Compliance

We build permissioned blockchain networks that enable secure, auditable international clinical data exchange while automating compliance with GDPR, HIPAA, and regional data sovereignty laws.
Chainscore © 2026
overview
CORE SERVICE

Smart Contract Development

Secure, audited smart contracts built for production on EVM, Solana, and Cosmos.

We architect and deploy mission-critical smart contracts for DeFi, NFTs, and enterprise applications. Our development process ensures security-first code that is gas-optimized and upgradeable from day one.

Deploy with confidence using battle-tested patterns from OpenZeppelin and Sealevel.

Our development lifecycle includes:

  • Formal Specification: Requirements mapped to Solidity or Rust architecture.
  • Security-First Coding: Adherence to best practices with automated vulnerability scanning.
  • Comprehensive Testing: Unit, integration, and scenario testing with forked mainnets.
  • Third-Party Audits: Coordination with leading firms like CertiK and Quantstamp.
  • Deployment & Monitoring: Mainnet deployment with 24/7 monitoring and incident response.

We deliver production-ready contracts in 2-4 weeks, backed by a 99.9% uptime SLA. Our engineers have deployed over 200+ contracts handling billions in TVL, specializing in:

  • ERC-20, ERC-721, and ERC-1155 token standards
  • Custom Automated Market Makers (AMMs) and lending protocols
  • Cross-chain bridges and interoperability layers
  • DAO governance and multi-signature systems
key-features-cards
BUILT FOR HEALTHCARE

Core Capabilities of Our Compliance-First Networks

We engineer permissioned blockchain networks specifically designed to meet the stringent regulatory demands of clinical data exchange. Our infrastructure ensures data integrity, patient privacy, and seamless auditability from day one.

03

Real-Time Audit Trail & Provenance

Every data access, consent change, and transaction is immutably recorded. Provides regulators and auditors with a tamper-proof ledger for complete traceability and compliance reporting.

Immutable
Ledger
Real-Time
Auditing
04

Multi-Jurisdiction Data Governance

Modular smart contracts for managing region-specific rules (EU GDPR, US HIPAA, APAC regulations). Enforce data residency policies and cross-border transfer mechanisms on-chain.

Modular
Rulesets
Geo-Fencing
Policies
05

High-Throughput Clinical Data Pipeline

Optimized for large-scale, sensitive datasets. Achieve sub-2-second finality for consent updates and data access grants without compromising network privacy or security.

< 2 sec
Finality
10k+ TPS
Private Network
06

Certified Node Operations & Security

All validator nodes are operated by vetted, accredited healthcare institutions. Networks undergo annual penetration testing and are built on ISO 27001-aligned security frameworks.

ISO 27001
Framework
Vetted Nodes
Operators
benefits
DELIVERABLES

Business Outcomes for Pharmaceutical & CRO Teams

Our blockchain-based platform for clinical data sharing delivers measurable results, accelerating trials while ensuring immutable compliance with global regulations like GDPR and HIPAA.

01

Accelerated Trial Timelines

Reduce patient data onboarding and site synchronization from weeks to days. Our immutable ledger provides a single source of truth, eliminating reconciliation delays between sponsors and CROs.

70%
Faster Data Unification
< 48 hours
Site Sync
02

Audit-Ready Compliance

Automate compliance logging for GDPR, HIPAA, and 21 CFR Part 11. Every data access, consent update, and amendment is cryptographically sealed on-chain, creating an unforgeable audit trail.

100%
Immutable Logging
Zero-trust
Access Model
03

Reduced Operational Cost

Eliminate manual data aggregation and costly third-party audit fees. Smart contracts automate data-sharing agreements and compliance checks, cutting administrative overhead.

40-60%
Lower Admin Cost
Automated
Contract Execution
04

Enhanced Data Integrity & Security

Patient data is pseudonymized and anchored on a permissioned blockchain. Tamper-evident logs and cryptographic proofs ensure data provenance and prevent unauthorized alterations.

End-to-end
Encryption
HIPAA-aligned
Architecture
05

Streamlined Sponsor-CRO Collaboration

Real-time, permissioned data sharing between all authorized parties on a unified platform. Eliminate data silos and version conflicts with synchronized, timestamped records.

Real-time
Data Access
Role-based
Permissions
06

Future-Proof Data Portability

Built on interoperable standards, our solution ensures trial data remains accessible and verifiable across systems and future regulatory frameworks, protecting long-term research value.

W3C
Standards-based
Regulatory Agile
Design
Why Blockchain for Clinical Data?

Chainscore vs. Traditional Data Management Systems

A direct comparison of infrastructure approaches for managing cross-border clinical trial data, highlighting the compliance, security, and operational advantages of Chainscore's blockchain-based solution.

Critical FactorTraditional Systems (e.g., Centralized DB, Cloud)Chainscore Blockchain Platform

Data Provenance & Audit Trail

Manual logs, prone to tampering/errors

Immutable, cryptographic proof of all data actions

Patient Consent Management

Static forms, difficult to verify and update across sites

Dynamic, revocable smart contracts with on-chain verification

Cross-Border Data Sovereignty

Complex legal agreements, high compliance overhead

Built-in compliance via programmable logic for GDPR, HIPAA

Real-Time Data Reconciliation

Batch processing, leads to latency and discrepancies

Single source of truth with sub-5-second finality across sites

Security Model

Perimeter-based (firewalls, access controls)

Cryptographic (zero-knowledge proofs, encrypted on-chain storage)

Audit Readiness for Regulators

Months of preparation, manual evidence gathering

Real-time, permissioned auditor access to verifiable ledger

Time to Deploy Compliant System

9-18 months

8-12 weeks with our compliant templates

Estimated Annual Compliance Cost

$250K-$1M+ (legal, security, audits)

$75K-$200K (managed platform + SLA)

Data Integrity Guarantee

Best-effort, relies on system trust

Mathematically verifiable via Merkle proofs and consensus

how-we-deliver
PREDICTABLE, AUDITABLE, AND COMPLIANT

Our Phased Delivery Methodology

We deliver compliant cross-border data sharing infrastructure through a structured, milestone-driven process. This ensures regulatory alignment from day one, reduces project risk, and provides clear visibility for your stakeholders.

01

Phase 1: Compliance & Architecture Design

We conduct a compliance gap analysis against GDPR, HIPAA, and country-specific data sovereignty laws. This phase delivers a technical architecture blueprint and a data governance model for your review and approval.

2-3 weeks
Typical Duration
100%
Regulatory Mapping
02

Phase 2: Smart Contract & Protocol Development

Our engineers build the core on-chain logic for data access consent, audit trails, and tokenized permissions. We implement zero-knowledge proofs for privacy and develop off-chain verifiers to ensure data integrity before on-chain commitment.

4-6 weeks
Development Sprint
OpenZeppelin
Security Foundation
03

Phase 3: Integration & Interoperability Layer

We build secure APIs and middleware to connect your existing clinical systems (EHR/EMR) to the blockchain layer. This includes developing oracles for real-world data and ensuring seamless interoperability with required healthcare data standards (HL7 FHIR).

3-4 weeks
Integration Window
HL7 FHIR
Data Standard
04

Phase 4: Security Audit & Compliance Validation

The complete system undergoes a rigorous security audit by a third-party firm. We execute a compliance validation run with synthetic data to generate evidence for regulatory submissions, ensuring the system operates as designed under governance rules.

2 weeks
Audit Cycle
CertiK / Trail of Bits
Audit Partners
05

Phase 5: Staged Deployment & Knowledge Transfer

We deploy the solution in a staged rollout, beginning with a controlled pilot. We provide comprehensive documentation, operational runbooks, and training for your technical team to ensure full ownership and long-term operational success.

1-2 weeks
Pilot Deployment
Full Handoff
Deliverable
06

Ongoing: Compliance Monitoring & Support

We offer SLA-backed infrastructure monitoring and proactive compliance updates. Our team tracks evolving regulations (like EU Data Act) and provides patches or upgrades to maintain your system's legal standing across jurisdictions.

99.9%
Uptime SLA
24/7
Monitoring
security
CORE SERVICE

Smart Contract Development

Secure, production-ready smart contracts built for scale and compliance.

We architect and deploy custom smart contracts that power your core business logic. Our development process is built on security-first principles, utilizing OpenZeppelin libraries and formal verification to mitigate risk. We deliver audit-ready code from day one.

From tokenization to complex DeFi protocols, we build the immutable foundation your application needs to operate with trust and efficiency.

  • Token Standards: ERC-20, ERC-721, ERC-1155, and custom implementations.
  • DeFi & DAOs: Automated market makers, staking pools, governance modules.
  • Enterprise Logic: Supply chain tracking, asset tokenization, verifiable credentials.
  • Key Deliverable: A fully documented, tested, and auditable codebase ready for mainnet deployment.
Cross-Border Clinical Data Sharing

Frequently Asked Questions

Get clear answers on how we ensure your clinical data platform meets global compliance standards like HIPAA, GDPR, and country-specific regulations.

We follow a 4-phase methodology: 1) Regulatory Mapping to identify all applicable laws for your target markets. 2) Architecture Design incorporating privacy-by-design principles (data minimization, pseudonymization). 3) Technical Implementation using on-chain access controls, zero-knowledge proofs for verification, and off-chain encrypted storage. 4) Audit & Documentation to produce the necessary Data Protection Impact Assessments (DPIAs) and compliance evidence. Our team includes certified privacy professionals.

ENQUIRY

Get In Touch
today.

Our experts will offer a free quote and a 30min call to discuss your project.

NDA Protected
24h Response
Directly to Engineering Team
10+
Protocols Shipped
$20M+
TVL Overall
NDA Protected Directly to Engineering Team