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myLaminin

myLaminin provides a unified, secure platform for Clinical Research Data Management (RDM) and general research needs. It covers every stage of the data lifecycle, from the initial setup to final publication. Additionally, it features a unique, patented Verifiable Credential technology protected in the US and Canada.

What myLaminin Does

myLaminin helps active research teams and institutions mitigate cybersecurity, data privacy, compliance, and logistical risks.

It is the only generalist RDM solution designed to support the complete end-to-end research data lifecycle, including team management, data collection, clinical trial operations, IRB/REB submissions, audit trails, data repository management, and dataset publication.

Key Features

Research Team Collaboration

Empower global research groups to partner safely through the use of granular permission settings and decentralized data control systems.

eSignature Agreements

Create and manage NDAs, intellectual property agreements, data-sharing agreements, and publication agreements through an integrated Adobe Acrobat Sign experience and 21 CFR Part 11 compliance.

Robust Data Collection

Securely manage PHI and PII data using medical ontologies, pre-built templates, and electronic participant consent forms.

Clinical Trial Management (CTMS)

Define protocols, track participants and follow-ups, manage delegation logs, team training certifications, and support PI eSignatures consistent with 21 CFR Part 11 with full ICH E6(R3) support and System Validaton Package with several significant AI-enabled features.

IRB/REB Support

Manage Research Ethics Board processes with support for multiple boards, institutional forms, institutional workflows, and calendar and email integrations.

Real-Time Audit Trail

Maintain a comprehensive audit trail of actions performed by every research team member.

Flexible Data Storage

Choose between secure cloud-based and on-premises data storage options with multi-site federated data management capabilities.

Data Sovereignty

Support FAIR principles and Indigenous Data Sovereignty, such as OCAP and CARE, through a complete Indigenous Data Sovereignty Technology Stack.

Verifiable Credentials

Issue and verify secure digital credentials with a USPTO- and CIPO-patented platform.

Security and Compliance

myLaminin is SOC 2 Type II certified and supports compliance with:

  • NIST SP 800-171
  • HIPAA
  • PHIPA
  • PIPEDA
  • GDPR
  • 21 CFR Part 11
  • ICH E6(R3)

myLaminin also uses blockchain and Web3 technologies to support data security and integrity. Its technology is protected by issued U.S. and Canadian patents.

Who Uses myLaminin

myLaminin is designed for clinical research coordinators, data managers, sponsors, academic researchers, research institutions, hospitals, and enterprise organizations across Canada and globally.

It is trusted by organizations including the Queen's University, Royal Military College of Canada, Ontario Ministry of Health, CANARIE, the Centre for Advanced Computing, Cardiac Institute of Research at Queen's, Basia Medical, and other medical device manufacturers, hospital systems and research institutes.

Pricing and Access

Pricing is available upon request.

To learn more or book a demonstration, visit mylaminin.net/contact-us.

Frequently Asked Questions

What is myLaminin?

myLaminin is a secure, cloud-based Clinical and Generalist Research Data Management (RDM) platform supporting the full lifecycle of active research projects—from project initiation through dataset publication. It also has a W3C compliant Verifiable Credentials solution that is patent-protected in both Canada and the US.

Who is myLaminin for?

myLaminin is designed for clinical trial management, sponsors, academic researchers, research institutions, hospitals, and enterprise organizations that require secure and compliant management of active research data.

Is myLaminin compliant with research data regulations?

Yes. myLaminin is SOC 2 Type II certified and supports compliance with NIST SP 800-171, HIPAA, PHIPA, PIPEDA, GDPR, ICH E6(R3), and 21 CFR Part 11.

Does myLaminin support clinical trials?

Yes. It offers a comprehensive, integrated Clinical Trial Management System (CTMS) that includes EDC form creation, data reporting, and protocol design. It facilitates seamless participant tracking, follow-up scheduling, and delegation logs. The system ensures PI eSignatures align with 21 CFR Part 11, manages training certifications, employs role-based access, and streamlines clinical trial operations with tools for payment and invoicing.

Does myLaminin support Indigenous Data Sovereignty?

Indeed. myLaminin aligns with OCAP and CARE standards for Indigenous Data Sovereignty, providing essential tools and frameworks for communities involved in diverse research initiatives.

How do I get started?

Visit mylaminin.net/contact-us to request more information or book a demonstration.

Key URLs

Last Updated

October 2026

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