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One platform for trusted data.
Built for compliance.

Manage documents, data, and workflows, in one secure, AI-enabled, regulatory compliant platform - built specifically for active research science, clinical trials, and digital trust.

Backed by

Collaborate

Enable secure collaboration across teams and organizations with granular permissions, automated workflows, and access controls.

How myLaminin Supports Your Work

Capture

Securely collect documents, data, identities, and records from people, systems, and organizations into a single trusted platform.

Verify

Prove the integrity of every action with CIPO and USPTO-patented cryptographic audit trails, e-signatures, and immutable compliance records.

Organize

Structure information into projects, workflows, and relationships, to create one centralized source of truth. 

Analyze

Transform trusted information into real-time dashboards, reports, insights, and decisions, all from the same platform.

Why one platform changes everything

Replace disconnected point solutions with one secure platform built for regulated information

Docs + Data + Workflows + Credentials → myLaminin

Built for Your Team

One Platform. Three Solutions.

Verifiable
Credentials

  • W3C credential issuance

  • Instant credential verification

  • Privacy-first trust networks

Clinical
Trials

  • Unified CTMS, EDC & eTMF

  • Sponsor portal with RBQM support

  • ICH E6(R3)+FDA 21 CFR Part 11 Compliance

Research Data
Management

  • National & Indigenous Data Sovereignty

  • Repository publishing with DOI support

  • Cross-institution collaboration

Trusted by the top 1%

Director Clinical Trial Operations,

Clinical Trial Support Unit

"We were able to establish and deploy our entire trial EDC forms - ready for use - in just one day. Our startup paperwork and site source file setup is 70% more efficient using myLaminin."

Clinical Research Nurse,

Academic Research Institute

"We love myLaminin’s visual indication of participant status. We can instantly see which forms need to be filled at each step, cutting our participant tracking effort in half."

Clinical Research Operations Lead,

Health Sciences Centre

"The integrated CtQs, QTLs, automated delegation logs, and audit trails in one solution gives us 95% more confidence in our audit readiness and regulatory compliance."

5

Permission-Aware Reporting

Live Analytics Without Compromising Security
Real-time dashboards and reports built directly on live data while automatically respecting every user's permissions.

4

Trust by Design

Immutable Audit Trails & Digital Integrity
Every action is cryptographically protected with immutable audit trails, digital signatures, version history, and traceable records.

3

Granular Access Control

Field-Level Security & Governance
Permissions down to the field, row, site, role, and project level.

2

Flexible Data Residency

Access to Global AWS Hosting
Store project data in either Canada, the United States, or wherever data residency is required with flexible residency and governance controls.

1

Unified Platform

Eliminate the Integration Tax
A single platform that unifies research data, documents, workflows, reporting, compliance, and clinical operations—without stitching together multiple products.

Everything You Need, Built In

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SOC 2 Type II

Rigorous standards for security, availability, and confidentiality.

Built to meet the highest standards

Certified & fully compliant

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21 CFR Part 11

FDA compliance for electronic records and signatures.

Our platform undergoes rigorous independent certifications to ensure the highest standards of data integrity and regulatory compliance.

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ICH E6(R3)

Global GCP standards for clinical trial design and conduct.

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Blockchain & Digital Trust

Blockchain-verified audit trails for immutable record keeping.

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PIPEDA

Compliance with Canadian privacy laws for personal data.

NIST SP 800-171

Cybersecurity frameworks for protecting sensitive information.

Self-assessed against

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Proactively aligned with leading industry frameworks to ensure broad institutional compatibility.

PHIPA

Ontario's health information privacy and protection act.

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GDPR

European standard for data protection and user privacy.

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HIPAA

US standard for protecting sensitive patient health information.

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Ready to power your next breakthrough?

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