Explore how Nonte supports diverse, high-impact research programs, from neurodegenerative disease tracking to multi-provincial cancer cohorts, by making research data reliable, structured, and regulatory-ready.

Use Cases :
Real Research, Real Impact

Use Cases: Real Research, Real Impact

Stories from our Clients

At Nonte, we’ve had the privilege of supporting groundbreaking research across disease areas, institutions, and study designs. These stories reflect the depth and flexibility of our platform, and the trust our partners place in us.

Whether you’re managing a single-site pilot or a multi-institutional program, we’re excited to bring that same expertise, care, and commitment to your study. Let’s explore what we can build together.

Neurology Research from Clinic to Cohort

Capturing longitudinal neurodegenerative data directly from a specialty clinic into a centralized research environment.

Ingests EMR data while preserving clinical structure
Supports complex CRF design reflecting real-world value sets
Enables transparent reporting across hospital and research workflows

Discover how we support clinical integration

Decentralized Trials for Parkinson’s Disease

Unifying data from wearables, EMRs, and CRFs in a decentralized trial setting.

Combines app-based, EMR, and manual data inputs
Builds interoperable datasets for remote participants
Streamlines compliance and analysis in DCT environments

Learn how we simplify remote trial data

Concept of application new technology in future medicine

Inter-Provincial Oncology Biobank Collaboration

Managing specimens and data across four biobanks and three genomics labs in different provinces.

Tracks samples from intake to sequencing
Supports distributed lab processes and data access
Provides a searchable specimen registry across all study sites

See how we connect biobanks to research goals

Antimicrobial Resistance Research at Scale

Supporting a five-institution, NIH-funded program with microbiome, omics, and process tracking tools.

Manages metadata, logistics, and multi-step lab workflows
Provides specimen ID and storage traceability
Organizes lab metadata for downstream analysis and sharing

Explore how we support complex study ecosystems

Longitudinal CDiff Surveillance Across 50 Sites

From legacy systems and REDCap to seamless, centralized lab and CRF data.

Migrates historical and current clinical-lab data
Supports multi-year study structures and process changes
Unifies study documentation for traceability and audit-readiness

Get in touch to hear how migration works

Healthy Volunteer Clinical Trial Data Management

Managing detailed CRFs, labs, and safety evaluations in a tightly scoped Phase I trial.

Creates customized forms for daily and event-driven assessments
Supports unified tracking of labs, AE reporting, and dosing
Enables self-service data access for sponsors and reviewers

Ask us how we scale from small studies to big impact

Frequently asked questions

Got questions? You’re not alone, here are a few our team hears all the time.

What is Nonte, in simple terms?

Nonte is a cloud-based platform designed to enhance data traceability and oversight in translational research. It connects study workflows, data points, and documentation into one audit-ready environment, ensuring that every aspect of your research is accurately tracked and easily accessible.

Will it replace my current systems?

No, Nonte is designed to integrate seamlessly with the tools you already use, such as REDCap, EDCs, and lab systems. This means you can enhance your existing workflows without the need to replace or overhaul your current systems. But if you are in the market for a new system, Nonte can replace current systems end to end if needed.

How hard is it to implement?

Nonte is quick to configure and doesn’t require major IT involvement. Most teams can be up and running in days, not months, allowing you to start improving your data management processes almost immediately.

What will this cost—and what do I save?

Pricing for Nonte is scalable based on study size and usage, designed to accommodate research budgets. By reducing errors, delays, and compliance issues, Nonte always saves more than it costs, providing a significant return on investment.

Who is already using it?

Nonte is being implemented by academic institutions, accelerators, and translational research programs in Canada, USA and the UK, including University of Houston, Atlantic Cancer Consortium, Houston Methodist, Aston University and many others. Our user base is growing rapidly, reflecting the platform’s effectiveness and adaptability.

Is this just for regulated clinical trials, or earlier too?

Nonte supports the entire translational journey from preclinical studies to regulatory submission and impact studies. It’s especially valuable in early-phase research, where traceability and structure are often lacking, ensuring that your data is robust from the outset.

How secure is my data?

Your data is encrypted, securely stored, and always under your control. Nonte is built with strict data governance and compliance in mind, ensuring that your information remains confidential and protected.

Book a personalized demo with one of our team members and discover how Nonte brings clarity, traceability, and control to your research data needs and workflow. We’ll walk you through the platform, answer your questions,and show you exactly how it fits your needs – from day one

Book a Demo

Use Cases :
Real Research, Real Impact