Accelerate Biotech Innovation
via Transparent, Trusted, and Secure Data Collaboration
Biotech's greatest breakthroughs are stalled not by scientific limits, but by organizational silos. Our enterprise-grade Blockchain-as-a-Service fosters trust and seamless collaboration to unlock progress.
We understand your journey
1/5,000
drugs reach the market out of thousands of potential compounds
10+
years average development from discovery to market approval
$2.6B
average cost per drug including failed attempts and regulatory costs
Discovery
2-5 years
100%
Preclinical
3-6 years
12%
Clinical Trials
6-9 years
5%
Regulatory Approval
1-2 years
1%
success-
rate
What’s Really
Causing the Delays?
Broken
collaboration
Unclear
data
Compliance
gaps
Drug Discovery & Preclinical Research
Your scientists are close to a breakthrough in AI-driven biomarker discovery. But progress stalls, not due to research, but due to datasets lacking clear, traceable provenance. This isn't a technical hiccup. It's a systemic risk.
Critical Challenges
Regulatory Approval Risk
Vulnerable research integrity
Preclinical Replicability
Biobank Oversight
Erosion of trust
Compromised Sample Integrity
The Solution
A unified clinical trial ecosystem where patient consent is dynamically managed, data from all sources is harmonized in real-time, and every event is immutably logged, creating a single source of clinical truth that:
Accelerates AI
readiness
Ensures
compliance
Safeguards IP
Reinforces
stakeholder trust
Clinical Development
Modern clinical trials are complex, data-heavy, and multi-centered, requiring trust, transparency, and operational integrity across sponsors, CROs, investigators, patients, and regulators. Sustaining this trust across stakeholders remains a core industry challenge.
Critical Challenges
Patient mistrust
Fragmented Data
Inefficient Consent Management
Expensive re-trials
Regulatory Audit Risks
The Solution
A unified clinical trial ecosystem where patient consent is dynamically managed, data from all sources is harmonized in real-time, and every event is immutably logged, creating a single source of clinical truth that:
Fosters patient trust and accelerates recruitment
Ensures data integrity across all trial sources
Streamlines regulatory audits and submissions
Empowers investigators with complete, real-time data
Commercialization
Post-launch drug recalls due to supply chain issues can cripple manufacturers. Siloed, fragmented data across vendors hinders traceability, raising compliance risks and revenue loss due to lack of visibility and delayed response.
Critical Challenges
Supply Chain Opacity & Counterfeit Risk
Maintaining Cold Chain Integrity
Inefficient Recall Management
The Solution
A transparent supply chain where every handover, temperature log, and quality check is captured on an immutable, shared ledger, creating a digital passport for every product that:
Enables rapid, precise, and targeted recalls
Fortifies patient safety and protects brand value
Guarantees product authenticity, eliminates counterfeits
Ensures end-to-end cold chain integrity
Blockchain: Powering Next‑Gen Biotech Breakthroughs
A typical biotech journey spans years. Delays mean lost revenue and slower access to critical therapies.
But what if you could shorten that timeline by even four months?
Extend Market
Exclusivity
Secure additional months of patent-protected sales, directly impacting top-line revenue
Enhance Drug
Success Rates
Improve the probability of successful phase progression through superior data integrity and faster, more confident go/no-go decisions.
Accelerate Time-to-Patient
Shorten the clinical-to-market timeline to deliver critical therapies to patients months ahead of schedule.
Biotech-Centric
Architecture
Ensure all data, from research to clinical trials and supply chain logs, is tamper-proof, timestamped, and fully traceable.
Built-In Regulatory
Compliance
Provides immediate compliance readiness with integrated support for industry regulations, minimizing operational risks and boosting stakeholder confidence.
Fast & Seamless
Integration
Connects with existing systems (LIMS, ERP, EDC) via developer-friendly APIs, enabling go-live in days, not months.
Blockchain-Powered Trust
for Verifiable Biotech
Your workflow doesn't change. Its integrity and verifiability do
FLEXBLOK is an enterprise-grade private blockchain-as-a-service platform that works with your existing systems. Think of it as the secure backbone that connects and validates the data your team relies on every day, making your processes inherently audit-ready.
Establish Unshakeable Data Integrity
Ensure all data, from research to clinical trials and supply chain logs, is tamper-proof, timestamped, and fully traceable.
Foster Trust-Based Collaboration
Enable secure, permissioned data sharing with internal teams, CROs, and academic partners, complete with an audit trail.
Automate and Streamline Compliance
Automate trial milestones and patient consent with smart contracts to reduce manual oversight and ensure audit readiness.
Accelerate Your Timelines
FLEXBLOK reduces data management friction and enhances collaboration, speeding up development cycles to bring innovations to market faster.
Case Studies & Use cases
Patient-Centric
Empowers patients with full control over their data
Unified Ecosystem
A single, transparent platform for all stakeholders.
Immutable Audit Trail
Guarantees data integrity for R&D and compliance.
Rapid Deployment
Foundational infrastructure live in eight weeks.
Verifiable Chain of Custody
An immutable, auditable log for every sample's journey.
Enhanced Research Credibility
Empowers researchers with undisputed data provenance.
Sovereign Health Identity
A portable, verifiable digital identity for every patient.
Consent-Driven Access
Patients control all data access via smart contracts.
Breach-Resistant Storage
Encrypted health records on a decentralized network.
Fuel Your Next Innovation, Not Your Legacy System Overheads
FLEXBLOK enables biotech teams to meet evolving industry demands with speed, security, and simplicity, without needing blockchain expertise.
Let’s talk through your biotech challenge, and show you how FLEXBLOK delivers.
What Industry Leaders Are Saying About FLEXBLOK?
We required a verifiable traceability system for our lymphoma samples without a long, complex build-out. Flexblok provided a low-cost, production-ready infrastructure in under eight weeks.
CTO
Europe’s Leading Academic Research Consortium
Our research process was constantly slowed down by teams working with different data. We’re so thankful to finally have one shared, trusted Infrastructure for everything, as it lets our scientists focus on the science, not the data.
CMO
French biotech developing precision antibody‑drug conjugates
We were seeing increasingly sophisticated check fraud attempts across our network. It’s a significant relief to have the platform's digital notary function, to provide the concrete, transaction-level proof needed to effectively mitigate those threats.
CEO
U.S. based Start-Up Specializing in Check Cashing
Manual data gathering for regulatory audits was a major resource drain for our quality team. This platform's ability to create and maintain an immutable, real-time audit trail has been a significant operational improvement.
CTO
Leading U.S.-Based Pharmaceutical
Our process for verifying training data was taking up way too much of the team's time. We needed to log everything without ripping apart our pipeline. FLEXBLOK's APIs helped us create that verifiable history for every dataset, and now our team can access it in real time.
Lead Engineer
UK-Based AI Orchestration Platform
The platform itself is powerful, but what stood out was the support during integration. The team felt like an extension of our own, responsive, knowledgeable, and genuinely invested in getting it right. That kind of partnership is rare.
CTO
A New York-based SaaS company
Frequently asked questions
Everything you need to know about the product and billing.
