Unqork for Life Sciences

Rapidly build enterprise-grade applications to make clinical trial processes more efficient, secure, and safe.

From the way clinical trials are run to patient services to regulatory operations, there are virtually no organizational life science functions that would not benefit from enhancements to digital engagement, execution, and innovation.

Using Unqork, life science companies are able to build portals to integrate and manage all medical affairs interactions with healthcare providers, including integration of data from CRM as well as intake tools to drive study startup, verifications, and regulatory operations—all without writing a single line of code.


Reduce total cost of ownership

Completely eliminate legacy code and effectively maintain your custom software throughout its lifecycle.


Get products to market faster

Accelerate the application development process with a single visual interface across the entire development stack.


Improve quality and reduce risk

Stop throwing requirements over the wall—your engineers, business owners, and analysts can collaborate more effectively with Unqork.

Life Sciences Solutions


Advanced Trial Monitoring

Digitize complex trial monitoring workflows for data review, patient recruitment, site evaluation, and more.


Study Startup & Site Onboarding

Build custom onboarding solutions to rapidly survey sites for feasibility information and link to downstream applications.


Patient Services Hub

Create a comprehensive patient experience, including seamless integrations with external systems and services.



Regulatory Operations

Codify and create end-to-end business processes to manage planning and compliance across a multitude of global stakeholders.



Digital Provider Collaboration

Manage all Medical Affairs interactions with providers, including integrating data from CRM as well as intake tools.

Featured Content

Discover our new Advanced Trial Monitoring solution

Unqork empowers organizations to efficiently conduct SDV—either remotely or on-site. Automated document scanning executes key tasks with machine efficiency, while robust Role-Based Access Control (RBAC) functionality ensures that trial data will only be reviewed by relevant trial monitors before being purged from the system.

Explore the solution
Left Floating Expert

Maintain compliance standards across your organization.

Featured Content

How No-Code Transforms Clinical Trial Management

In the following eBook we will explore two key ways no-code is being used to accelerate transformation in the life sciences sector.

read the ebook

Welcome to the future of life science application development.

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