OpenEDC becomes Livla 🎉 To the blog post →

Clinical trials and medical research

Livla is an easy and secure way to conduct clinical trials digitally. GCP, GDPR, and HIPAA compliant.

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The Livla Cloud is available now!

Developed in Germany, hosted in the Telekom Cloud. Try the app or request a demo.

Application areas

From thesis to clinical trial

Livla is the ideal solution for all types of research projects. From surveys during a doctoral thesis, to clinical outcomes study, to multi-centric studies. The modular concept allows the solution to be customized for every requirement.

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Clinical trials

Livla supports clinical research organizations (CROs) as well as medical device and pharmaceutical manufacturers in conducting clinical trials with a validated system. Fully AMG, MPG, DSGVO, GCP and HIPAA compliant.

Outcomes studies

Clinics and practices can use Livla to evaluate and continuously improve the outcome of their therapies. An app for patients allows user-friendly and digital follow-up. Interactive statistics provide insights in real time.

Registers

Livla enables university hospitals, institutes and other research institutions to conduct large longitudinal and multi-centric trials such as registries and epidemiological studies. With the option of distributed data storage.

Doctoral thesis

Students and individual researchers can use Livla locally on their own computers – without installation or registration. Surveys are easy to set up in compliance with the data protection regulations.

Features

A Variety of opportunities

Livla offers you all the essential functions to implement your research project quickly and easily.

Simple form creation

Livla offers an interactive, easy-to-understand form editor. Type in questions and pre-defined answer options in a natural way. See what the finished form looks like at any time. Create multilingual forms with real-time validations, branching / conditional logic, file uploads and much more.

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Reports and insights

Livla allows you to create powerful, highly interactive reports. Simply filter data with one click and combine multiple filters until you see the data selection you want. You can then easily export this selection, analyze it further with other statistical tools or share it with colleagues.

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Compliant with GCP

Livla complies with all legal requirements of Good Clinical Practice (GCP). View the audit trail that records all changes in the data set. Create, assign and monitor queries for the highest data quality. And use the granular roles and rights system to define user access permissions.

Livla Screenshot

More features

Livla offers many features to support you with your study.

Pseudonymization

Manage all participants of your trial – also completely pseudonymized if required.

Randomization

Coming soon: Different methods for the automatic randomization of subjects.

Document management

Revision-proof documents for patient consents, SOPs, wikis or similar.

Multi-center studies

Creation and management of multiple sites for distributed, multi-center studies.

Events and visits

Grouping of related forms for longitudinal studies and research projects.

Repeating data

Patient diaries or medication lists with an arbitrary number of repetitions.

Excel und CSV Import

Existing data can be cleansed, standardized and imported during a guided process.

Reason for change

Specifying a reason for data changes - in accordance with the GCP regulation.
Livla Teamphoto

Vision

Our vision

We want to be far more than just an EDC system. With Livla, we want to create a research platform that allows everyone around the world to use our product in a few seconds without lengthy sales loops, registration obligation or necessary expert knowledge. We strive to enable the collection of more qualitative data, the connection of data and, ultimately, the improvement of medical care.

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Practical experiences

We are advocates for academic research and provide institutes with an open, customizable and flexible solution for diverse research projects.

“The major advantages of Livla for us are user-friendliness, extensibility and interoperability. By supporting the CDISC ODM data standard, we can export and import both metadata and clinical data in a widely recognized format.”

Prof. Dr. Martin Dugas
University Hospital Heidelberg

“Decentralized data storage and record linkage is a vital factor for us. We use it to implement federated projects without disregarding the needs of the participating sites. Each clinic retains control over its data – and yet comprehensive monitoring is possible with Livla.”

Prof. Dr. Julian Varghese
University Hospital Münster

Get in contact

You want to be one of the first to use the new Livla app for your research? Then get in touch and we will introduce you to our solution.