Live Study Management

Minimise time lost to mid-study changes with the ultimate in adaptive trial platforms

Get started

Live Study Management

Minimise time lost to mid-study changes with the ultimate in adaptive trial platforms

Get started

Live Study Management

Minimise time lost to mid-study changes with the ultimate in adaptive trial platforms

Get started

Mid-study changes are inevitable. Unlike hard-coded platforms, Huma’s highly adaptable platform is designed with flexibility in mind to enable real-time modifications and additions to study protocols without having to go back to the drawing board.

Mid-study changes are inevitable. Unlike hard-coded platforms, Huma’s highly adaptable platform is designed with flexibility in mind to enable real-time modifications and additions to study protocols without having to go back to the drawing board.

Mid-study changes are inevitable. Unlike hard-coded platforms, Huma’s highly adaptable platform is designed with flexibility in mind to enable real-time modifications and additions to study protocols without having to go back to the drawing board.

Mid-study changes are inevitable. Unlike hard-coded platforms, Huma’s highly adaptable platform is designed with flexibility in mind to enable real-time modifications and additions to study protocols without having to go back to the drawing board.

Quicker changes with real-time configurability

Unlike other platforms, Huma is designed to be highly flexible to changing requirements, providing unparalleled configurability.This means that required, approved trial changes can be made immediately, with minimal time needed for User Acceptance Testing due to our intuitive UX design.

Self-serve or account managed change orders

We’ve designed our platform to be easy and intuitive to modify protocol changes and trial variations. Make your own changes directly in our configurable platform or use Huma’s expert team to make the changes for you.

Regulatory, safety and compliance
Regulatory compliance
International medical device standards
QMS & info security management
Technical documentation
Regulatory
compliance
International medical device standards
QMS & info security management
Technical documentation
Regulatory compliance
International medical device standards
QMS & info security management
Technical documentation
Regulatory compliance
International medical device standards
QMS & info security management
Technical documentation
Keep participants informed about the latest protocol changes

One challenge of trial changes is keeping participants in the loop. With Huma, you can easily choose which participants and participant cohorts will be able to see updates to protocols and testing regimes. As well as publishing updated trial guidance in the “Learn” module.

Increasing clinical trial success rates with adaptive technology

Fixing the foundations: building a solid evidence base for digital healthpp

Take the next step

Tell us what you’re working on and what you need from Huma to move forward.

Take the next step

Tell us what you’re working on and what you need from Huma to move forward.