FLEXBLOK - Accelerate Biotech Innovation

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.

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No sales conversation just pure tailored insights

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

The Traditional Journey
discovery
Discovery

2-5 years

100%
pre-clinical
Preclinical

3-6 years

12%
phase1
Clinical Trials

6-9 years

5%
phase2
Regulatory Approval

1-2 years

1%

success-rate

What’s Really
Causing the Delays?

broken
Broken
collaboration
broken
Unclear
data
broken
Compliance
gaps

Easy to miss, expensive to ignore. Let’s trace and fix it.

Drug Discovery & Research
Clinical Development
Commercialization

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
Auditors and regulatory bodies demand traceability, accountability, and ethical compliance.
Vulnerable research integrity
Fragmented consent records, incomplete processing histories, and missing metadata expose your work to invalidation.
Preclinical Replicability
Disconnected data undermines reproducibility, threatening scientific and financial credibility.
Biobank Oversight
Unverifiable consent and access logs expose your research to regulatory fines and public distrust.
Erosion of trust
The inability to prove data integrity erodes trust among donors, ethics boards, collaborators, and funders.
Compromised Sample Integrity
Genetic samples lacking verifiable provenance regarding their origin, consent, and handling history introduce fundamental uncertainty into subsequent research and actions.

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:

rocket
Accelerates AI
readiness
insurance
Ensures
compliance
safeguard
Safeguards IP
like
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
Lack of trust in data privacy, especially among diverse groups, significantly impedes clinical trial enrollment. Without transparent and verifiable data mechanisms, recruitment suffers, delaying timelines and undermining the generalizability of drug efficacy.
Fragmented Data
Critical data scattered across disparate systems (EDC, CRO databases) creates inefficiencies, leading to critical decisions based on incomplete information. This results in costly errors, audit findings, and delayed regulatory submissions.
Inefficient Consent Management
Traditional paper-based consent limits patient control and transparency over data use. This restricts recruitment efforts and reduces inclusivity crucial for representative clinical evidence.
Expensive re-trials
Maintaining protocol adherence and data integrity is paramount. Deviations, entry errors, and consent management issues compromise data quality, potentially invalidating trial sites, forcing expensive re-trials, and directly impacting approval pathways.
Regulatory Audit Risks
Incomplete documentation, fragmented audit trails, and cross-system data inconsistencies heighten exposure to regulatory findings. Such gaps undermine data credibility, delay marketing authorizations, and compromise the acceptability of clinical evidence by health authorities.

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:

rocket
Fosters patient trust and accelerates recruitment
insurance
Ensures data integrity across all trial sources
safeguard
Streamlines regulatory audits and submissions
like
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
Traditional pharmaceutical supply chains that lack granular, end-to-end visibility are vulnerable to counterfeits. This endangers patients, exposes your company to massive liability, and undermines years of R&D investment.
Maintaining Cold Chain Integrity
For biologics, an unverifiable break in the cold chain compromises efficacy and safety. This failure results in ineffective drugs, wasted inventory, and a direct threat to patient health and your company's financial stability.
Inefficient Recall Management
The inability to quickly and precisely trace affected batches due to fragmented tracking systems severely hampers recall efforts, amplifying public health risks, increasing financial penalties, and severely damaging your market standing.

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:

rocket
Enables rapid, precise, and targeted recalls
insurance
Fortifies patient safety and protects brand value
safeguard
Guarantees product authenticity, eliminates counterfeits
like
Ensures end-to-end cold chain integrity

Time is Your Most Valuable Asset

A typical biotech journey spans years. Each day of delay in a clinical trial isn't just a missed milestone; it's lost revenue and delayed patient access. What if you could shorten that timeline by 4 months? This acceleration can create a powerful strategic advantage:

Traditional Timeline vs
FLEXBLOK Timeline

4+ Month

Regulatory Prep Saved

30%

Faster Trial Audits

99.9%

Data Integrity
reason

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.

Why are Biotech Firms Turning to FLEXBLOK?

Biotech-Centric
Architecture

Ensure all data, from research to clinical trials and supply chain logs, is tamper-proof, timestamped, and fully traceable.

Built-In Compliance

Provides immediate compliance readiness with integrated support for industry regulations, minimizing operational risks and boosting stakeholder confidence.

Modular & Scalable Setup

Allows for pilot programs or single use cases, then scales across R&D, clinical, and commercial functions without vendor lock-in.

Fast & Seamless
Integration

Connects with existing systems (LIMS, ERP, EDC) via developer-friendly APIs, enabling go-live in days, not months.

Case Studies & Use cases

Secure Patient Data
Management

Protect sensitive patient records and genetic profiles through decentralized storage and consent-driven access. With Flexblok, data is encrypted, verifiable, and controlled by the patient — ensuring privacy without compromising collaboration.

Read Story read

Decentralized Clinical Trial
Management

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Read Story read

Automated Regulatory
Compliance in Healthcare

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Read Story read

100%

Patient-controlled consent through smart contracts

Zero

Data leaks in trial simulation

Multi-site

Compliance with HIPAA, GDPR, and beyond

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leapyear
leapyear

Ready to Transform Your Data Pipeline?

FLEXBLOK empowers biotech teams to meet the evolving industry expectations with speed, security, and simplicity without the burden of knowing about blockchain infrastructure from scratch.

Let’s talk through your biotech challenge, and show you how FLEXBLOK delivers.

Love the simplicity of the service and the prompt customer support. We can’t imagine working without it.

Amélie Laurent

Product Manager, Wildcrafted

Frequently asked questions

Everything you need to know about the product and billing.

How can blockchain specifically solve data provenance issues in AI?
A: Blockchain creates an immutable, timestamped ledger for every piece of data and its transformations. This means you have a verifiable, unalterable history of your data's origin, who accessed it, and how it was changed. For AI, this ensures the integrity of training data, helps identify biases at the source, and makes auditing data straightforward, directly addressing data provenance uncertainty. Keywords: blockchain AI data provenance, immutable data ledger AI, AI training data integrity, verifiable data history AI.

Keywords: blockchain AI data provenance, immutable data ledger AI, AI training data integrity, verifiable data history AI.

What is AI model lineage, and how does blockchain enhance it?
A: AI model lineage is the documented history of an AI model's development, including datasets, code versions, hyperparameters, and pre-trained components. Blockchain enhances this by storing each step and artifact of the model's lifecycle as a tamper-proof record. This ensures complete traceability from a deployed model back to its origins, improving reproducibility, accountability for model behavior (like bias), and easier debugging.

Keywords: AI model lineage blockchain, traceable AI models, reproducible AI blockchain, blockchain for AI model versioning.

How does blockchain contribute to Explainable AI (XAI) and decision attribution?
A: While blockchain doesn't inherently make models explainable, it provides a secure and immutable infrastructure to log the inputs, outputs, and explanatory artifacts from XAI tools. This creates a verifiable audit trail for AI decisions, making it possible to reliably trace why a specific decision was made and attribute it to specific data or model versions. This enhances accountability and trust in AI outcomes. Keywords: blockchain explainable AI, AI decision attribution blockchain, auditable AI decisions, responsible AI blockchain.

Keywords: blockchain explainable AI, AI decision attribution blockchain, auditable AI decisions, responsible AI blockchain.

Can blockchain improve the security of AI models and data?
Blockchain's decentralized and cryptographic nature enhances security by making data and model records tamper-evident and resistant to unauthorized changes. It can secure the storage and access to sensitive training data, protect the intellectual property of AI models by proving lineage, and ensure that only authorized versions of models are deployed.

Keywords: blockchain AI data security, secure AI models blockchain, decentralized AI data, AI intellectual property protection blockchain.

Is integrating blockchain into existing AI workflows complex?
A: While it can seem daunting, platforms like Flexblok (Blockchain-as-a-Service) are designed to simplify this integration. Flexblok offers APIs (like Data Tracing API, Document API) and tools that allow AI developers to incorporate blockchain functionalities without needing deep blockchain expertise, focusing on easy adoption and interoperability with existing AI pipelines.

Keywords: Blockchain as a Service AI, easy blockchain integration AI, AI workflow blockchain.

What are "smart contracts," and how are they relevant for AI on the blockchain?
A: Smart contracts are self-executing contracts with the terms of the agreement directly written into code. They run on a blockchain, becoming transparent, immutable, and automated. In AI, smart contracts can automate processes like data access permissions based on predefined criteria, royalty distribution for AI model usage, or even trigger actions based on AI model outputs in a verifiable way.

Keywords: smart contracts AI blockchain, automated AI governance, blockchain AI automation, decentralized AI applications.

Does using blockchain for AI impact scalability or performance?
A: This is a valid consideration. While early blockchains had scalability limitations, modern enterprise blockchain solutions like Flexblok are designed for high throughput and scalability. The specific impact depends on the blockchain architecture and how it's integrated. For AI lineage and provenance, not all data needs to be on-chain; often, hashes and critical metadata are stored, balancing integrity with performance.

Keywords: scalable blockchain for AI, AI performance blockchain, enterprise blockchain AI, Flexblok scalability.

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