Solutions / Clinical Validation & Industry

Strategic program

From promising idea to credible clinical evidence.

A governed pathway for hospital-based validation, academia–industry collaboration and transition into clinical trials.

See the modules

Strategic program. The modules on this page are planned or in development and are not yet generally available. Talk to us about timing and pilots.

The problem

What goes wrong today.

Promising academic work and new technologies often lack a clear path to hospital-based validation. Industry struggles to find the right investigators and sites, and institutions struggle to collaborate without losing oversight.

Who it is for

  • Innovators and academic teams
  • Pharma, MedTech and CROs
  • Hospitals and investigators
  • Research Offices

What MRB does

What MRB is designed to do.

MRB is being developed to help teams define the evidence question, find suitable sites and investigators, run validation studies through the proper ethics pathway, and move into My Trial Board (MTB) when a project becomes a formal clinical trial.

Illustrative interface, not a product screenshot.

Key capabilities

Modules in Clinical Validation & Industry.

Strategic program

Clinical Validation Services

Hospital-linked clinical evidence for technologies, products and interventions.

  • Clinical question and evidence-gap definition
  • Hospital, site and investigator matching
  • Validation-study design support
  • Evidence report and next-step recommendation
Strategic program

Industry Collaboration

Connect the right research question with the right expertise.

  • Research-interest and expertise profiles
  • Collaboration opportunity posting
  • Investigator-initiated study pathways
  • Controlled communication and document exchange
Strategic program

My Trial Board (MTB) Integration

When research becomes a clinical trial, move into MTB without starting from zero.

  • Hand-off from MRB project to MTB trial record
  • Re-use of investigator and institution information
  • Protocol and ethics continuity where applicable

Typical workflow

How a project moves through it.

  1. Define the evidence question
  2. Design the protocol
  3. Match site and investigator
  4. Ethics pathway
  5. Run the study
  6. Evidence report

Outputs

What you end up with.

  • A defined evidence question and study design
  • Matched sites and investigators
  • A clinical evidence report
  • A continuous research-to-trial pathway

Institutional value

What the institution gains.

  • Structured academia–industry collaboration
  • Institutional oversight retained throughout
  • Sponsored research opportunities for investigators
  • A route from validation into formal trials

Related solutions

Where the record goes next.

  • Expanding

    Grants & Innovation

    Match projects to funding, run structured grant calls, and route promising ideas toward IP, incubation and partners.

    Grant Assist & Funding Directory · Funder & Grant-Program Management · Innovation Hub, IP & Marketplace

    Explore Grants & Innovation
  • Future program

    Evidence & RWE

    A future evidence layer for registries, real-world evidence, implementation research and public-health intelligence.

    Registries & Real-World Evidence · Public Health & Implementation Research · Preventive Health & Population Intelligence

    Explore Evidence & RWE

Next step

Build a connected research ecosystem for your institution.

See how MRB fits your departments, your Ethics Committee and your Research Office.

Contact us

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