Setting standards in clinical trials with our unified software solution

Learn, Collaborate, and Report in Real-time

NAll clinical trial tools in one place
NSingle unified database
NComprehensive visual reporting
NFull functionality and inbuilt AI features

Setting new standards in clinical trials with our unified software solution

Learn, Collaborate, and Report in Real-time

NAll clinical trial tools in one place
NOne cohesive system
NFull functionality and inbuilt AI features

Industry changing unification features

Unleash infinite functionality within one system

In the world of clinical studies, sponsors, CROs or academia are dependent on multiple separated software tools, which in general are not natively connected. Wemedoo makes the trial software mess a thing of the past.

oomnia unifies all trial tools in one system: EDC with a drag and drop eCRF builder, eCOA, ePRO and eConsent for even more data entry points, a built-in RTSM, a fully fledged CTMS to overlook all trial data in real time, and an eTMF to meet all regulatory requirements. The unification of all trial tools means: one web-based login, one time data entry, one database, and one user interface for a smooth trial workflow.

oomnia has all functionalities that you would expect from each single tool and more. Add infinite users, sites and trials, as well as real-time insights, and inbuilt AI features. Realize any trial type and scale your research to unprecedented levels.

Centralize and simplify clinical trials

Unify your clinical trial tools on a single platform. Simplify data management and enhance collaboration now.

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Major unification features

Explore advanced connectivity options

Experience the benefits of a truly unified platform. Our major unification features bring together all the tools and data you need to streamline clinical trials and enhance collaboration. Explore the sections below for detailed information on how our unification capabilities can transform your research processes.

All Clinical Trial Tools in One Place

Simplify clinical trial management

Our unified clinical trial software oomnia provides all the necessary tools for managing clinical trials, streamlining processes, and enhancing efficiency.

Integrated platform

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All necessary tools are accessible for managing clinical trials within a single software platform, reducing the need for multiple applications.

Comprehensive suite

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oomnia includes features for study design, patient recruitment, data collection, monitoring, and reporting.

Centralized access

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Our platform features easy navigation between modules such as EDC (Electronic Data Capture), CTMS (Clinical Trial Management System), and ePRO (Electronic Patient Reported Outcomes) without leaving the platform.

Unified user interface

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oomnia comes with a consistent and intuitive user interface across all tools to enhance user experience and minimize training requirements.

Interoperability

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Our software offers a seamless integration with external systems such as EHRs, LIMS, and regulatory submission platforms to streamline operations.

Illustration shows all oomnia clinical trial software tools.

One Database

Ensure consistency and integrity of your data

Having a single, unified database for clinical trials enhances data management, improves efficiency, and ensures data integrity.

Centralized data repository

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oomnia allows to store all clinical trial data in a single, secure database to ensure consistency and ease of access.

Data integrity

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It is possible to maintain high-quality, validated data with robust audit trails and version control.

Real-time data access

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Our system enables real-time access to up-to-date trial data for all authorized users, facilitating timely decision-making.

One login

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Simplified user access is granted with a single sign-on (SSO) feature, allowing users to log in once to access all functionalities and data.

One-time data entry

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oomnia ensures that data entered once is available across all modules and tools, preventing the need for repeated data entry and minimizing the risk of errors.

Smooth Workflow

Create a cohesive and efficient trial environment

A smooth workflow in clinical trial management is vital for maximizing efficiency and ensuring successful outcomes. See what key components oomnia offers to ensure a sleek worflow.

Automated processes

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Our clinical trial software automates repetitive tasks such as patient scheduling, data entry, and monitoring alerts to enhance efficiency.

Streamlined communication

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oomnia facilitates seamless communication among study teams, sponsors, and sites with built-in messaging and collaboration tools.

Task management

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Our system utilizes task management features to assign, track, and manage tasks across different teams and roles, ensuring accountability and timely completion.

Regulatory compliance

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Built-in compliance checks and workflows ensure adherence to regulatory requirements, reducing the risk of non-compliance.

User-friendly design

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Intuitive design and easy navigation support smooth workflows, reducing the learning curve and enabling users to focus on critical trial activities.

Our proof of quality

We are ISO 9001 and ISO 27001 certified. Our commitment to robust information security and superior quality management is at the core of our innovative solutions, ensuring reliable and efficient trial management for our clients.

Immediate benefits with a unified system

Save your time and energy with our all-in-one solution

Trial efficiency goes up, while your costs go down. Reduce administration, programming, data reconciliation, data entry and analysis, and much more. Spend more time for quality assurance, reduce risks and improve your trial success rate.

Infrastructure costs reduced

Personnel costs reduced

Trial efficiency increased

CURIOUS?

Explore the full spectrum of our unified clinical trial tools through an insightfull demo call conducted by our esteemed oomnia experts.

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