Start your study in 2-4 weeks on our modern EDC software

  • Easy to use

  • Highly configurable EDC

  • Automate EHR and biomarker data imports

  • Site-based, hybrid & decentralized trials

  • ISO, HIPAA & Part 11 compliant

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IMPROVE PATIENT DIVERSITY

Run site-based, hybrid, and decentralized clinical trials

Hybrid and decentralized clinical trials enable diverse patient populations to participate in your study. Many competitors claim to support these trial types, but they lack the engaging patient experience and self-service options to onboard patients from anywhere.
  • Recruit patients from underrepresented groups

  • Trials with fewer visits can recruit further from study sites

  • Studies with no site visits can recruit from anywhere

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CONNECTED DEVICES

Upgrade your protocol with digital biomarkers

Measure heart rate, blood pressure, blood glucose, weight, temperature, activity, sleep, SpO2, and many other digital biomarkers within your study’s ePRO patient app. Apply evidence-based algorithms to calculate metabolic age and other patient health scores.
  • Enrich your study with biomarker data from 260+ devices

  • Simplify data collection with direct device connections

  • Identify patterns between different digital biomarkers

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REAL WORLD DATA (RWD)

Import patient medical records and labs—without data entry

Medical records and labs help you identify new patterns that inform current research and future studies, but traditional methods of collecting this data are time-consuming and expensive. Automatically retrieve complete patient histories without the need for offline health records requests and data entry.
  • Let patients request their medical records

  • Fetch records once or multiple times

  • Eliminate manual requests and data entry

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Trust, security and compliance

Mahalo is ISO27001 and ISO9001 certified and strictly adheres to FDA 21 CFR Part 11,
ICH E6 GCP, GDPR, and HIPAA guidelines.

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TIME-SAVING eCONSENT

Recruit, screen, and consent patients—in minutes

Recruit patients from a landing page (or in-person), pre-screen them with a few quick questions, and collect eConsent signatures in a single workflow. Mahalo is the only Part 11-compliant EDC system that saves your research team time so that you can reach your recruitment goals faster.
  • Simplify your study’s registration process

  • Consent patients in-person or virtually

  • Capture CFR Part 11 compliant eConsent signatures

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PATIENT-CENTRIC ePRO

Improve data quality with irresistible ePRO questionnaires

Collect better quality data and more of it with our simple and engaging ePRO questionnaires. With Mahalo, patients are automatically reminded about ePROs and other data collection tasks at the exact moment when the information is freshest.
  • Remind patients about recurring questionnaires

  • Collect answers on any device

  • Improve data quality

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Collect more and
better quality data with
our Platform

Get a Quote
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Switching to Mahalo Health's clinical trials platform has been a game-changer for our research team! The ease of use and ability to collect real-world data from various sources has significantly boosted our patient engagement and data quality. 


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Hannah Wallace

Clinical Research Coordinator
DATA PERMISSIONS

Assign user roles to blind researchers

Limit feature and data access by user role to blind principal investigators (PIs) while allowing other roles like research coordinators to access personal details to schedule appointments. Your study administrator can easily add and update user roles before publishing your study.
  • Configure user roles and access permissions

  • Add site monitors, research coordinators, PIs, and more

  • Set who can view personally identifiable information (PII)

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CONFIGURATION INCLUDED

Start up faster for less

While our software is easier to learn and use than competitors, we waive our eCRF and ePRO configuration service fees for all new customers. Just share your protocol and questionnaires, and our white-glove configuration team will take care of the rest.
  • Complete study startup faster

  • Study configuration services included

  • Start recruiting sooner

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Launch your study and change
patient behavior on one platform

Mahalo is the first digital health tool that enable you to study behavior
change.

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Accelerate your clinical trials
with our prebuilt solutions

Randomization

Define different block sizes with optional stratification in our variable block randomization module.

Adverse Events & Con-meds

Track adverse events, concomitant medications, and the reasons why patients drop out of your study.

Queries

Ask, manage, and resolve queries from a simple filterable list. View the specific query you’d like to resolve in a single click.

Data Dictionary & Exports

You can export your data dictionary or data for your entire study anytime in CSV format. Our APIs allow for third-party integrations.

Site Monitors & PIs

Site monitors and PIs have data access permissions and extra sign-off features to approve all study data.

Audit Trail

The audit trail follows Good Clinical Practice and tracks every user action to ensure your data integrity and mitigate risks.

©2024  Mahalo Digital Ventures, Inc.