Clinical Trials

Clinical insights at your fingertips

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Wemedoo Clinical Research Approach

Our pioneering clinical research approach to data collection and management revolutionizes healthcare and enhances patient outcomes through a multidisciplinary, innovative, and collaborative methodology that leverages cutting-edge technologies and upholds rigorous scientific practices.

Our clinical research approach is built on three pillars

Software

Innovative software for planning, collecting, and analyzing clinical and workflow data as well as improving operational study management and oversight.

Services

Comprehensive services portfolio, encompassing all stages of the clinical trial life cycle to provide high-quality results.

Global Capabilities

Innovative solutions with global reach to enhance clinical trials, including real-world data integration.

oomnia Unified Clinical Trial Software Solution

Oomnia Clinical Research image

oomnia is a comprehensive solution for managing multinational, traditional, decentralized, and synthetic clinical trials, ensuring high data quality while enabling precise process and document management.

Checkmark icon Reduce costs
Checkmark icon Reduce time to market
Checkmark icon Improve data quality
Checkmark icon Improve patient outcomes
EDC

EDC

Collect, clean, and review clinical trial data efficiently

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ePRO & eCOA

ePRO & eCOA

Streamline data collection directly from patients and physicians to ensure highest data quality

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RTSM

RTSM

Automate randomization and investigational product supply management directly within the eCRF

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CTMS

CTMS

Oversee and manage your clinical trial effectively and efficiently with full integration across all Oomnia modules and customized dashboards

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eTMF

eTMF

Digitally capture, manage, share, and store essential documents and content

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eConsent

eConsent

Increase flexibility for patients while improving data quality and operational efficiencies with native EDC integration

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Medical Coding

Medical Coding.

Assign medical codes directly in the eCRF during the data collection stage

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Safety

Safety

Automate adverse event management with native EDC integration

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Lab Management

Lab Management

Integrate central and local laboratory reference ranges, sample management, and data collection

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Imaging

Imaging

Collect image assessment results directly in the eCRF, integrated in the analytical data set

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Query Management

Query Management

Reduce the number of manual queries by over 60% through dynamic automated data cleaning

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eSource

eSource

Collect data directly through EMR/EHR integration

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eArchive

eArchive

Curate and store your data along the entire clinical trial process life cycle

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Medical Device Data Integration

Medical Device Data Integration

Integrate data feeds from wearables and centralized vendor databases directly into the eCRF

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Services

Oomnia Clinical Research image

We provide comprehensive support and guidance throughout identification of requirements, protocol development, data management, statistical analysis, and final reporting to ensure your success.

Checkmark icon Greater efficiency
Checkmark icon Higher accuracy
Checkmark icon True transparency
Checkmark icon Customer success

Clinical Trial Professional Services

Consultation

Consultation

Customize your consultation services according to your clinical trial and business needs

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Data Management

Data Management

Generate high-quality, reliable, and statistically sound data to support your clinical trial

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Pharmacovigilance

Pharmacovigilance

Automate adverse event management to bolster patient safety surveillance in real-time

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Biostatistics

Biostatistics

Unlock the true potential of your clinical trial data with accurate analyses and visualization

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Medical Writing

Medical Writing

Let our highly qualified experts accelerate your trial to final submission-ready documents

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oomnia Customer Success

Advisory and Scoping

Advisory and Scoping

Leveraging insightful collaborative discussions, we tailor the system to amplify clinical trial design and data collection to align with your objectives

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Implementation

Implementation

We set up Oomnia according to your requirements and connect all systems

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Training

Training

We ensure your team is provided with relevant trainings and associated documentation throughout the trial

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Support

Support

We provide 24/7 support to ensure your needs are met

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Global Capabilities

Global Capabilities Network image

Get enhanced and innovative global solutions through highly qualified, globally experienced, and knowledgeable local experts.

Checkmark icon Unlimited possibilities
Checkmark icon Global reach
Checkmark icon Unique solutions
Checkmark icon Unique results
Real-World
Data

Real-World
Data

Integrate real-world data to support your clinical trial

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Clinical Trial Services

Clinical Trial Services

Conduct global trials in a cost efficient manner

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Specialty Services

Specialty Services

Address special topics with tailored specialty services

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Rare Diseases

Rare Diseases

Expand your global reach to include underserved patients and regions through our alliance of CROs

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Experience unique functionality that will change your world

Interoperability icon

Interoperability

All solutions are semantically inter-operable and ensure seamless data exchange with other internal and external systems.

Reusability icon

Reusability

Each created object is available to you at any time and can be used again, even in other studies.

Flexibility icon

Flexibility

The system is uniquely flexible and can be easily adapted to your changing needs without downtime, even in an ongoing study.

Compatibility icon

Compatibility

The CDISC standard is integrated into every data field throughout the entire process, starting with the very first data entry.

Uniqueness icon

Uniqueness

Unparalleled eCRF integration capabilities, including RTSM and centralized laboratory management, with real-time downloadable metrics and visualizations.

Generate prolific insights from your clinical trials with a truly interoperable platform.

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