About Oomnia
Oomnia is a clinical trial software/platform from Wemedoo that provides clinical trial tools. It combines eConsent, unification, and professional assistance so users can access a unified solution for their clinical trials. The platform supports interoperability and allows access from anywhere, making it easier to manage various phases of clinical research. Oomnia is designed to cater to the needs of clinical trial professionals, offering a comprehensive approach to data management and collaboration among teams. Key capabilities: eConsent Unification Professional Assistance Interoperability Access from Anywhere Best for: clinical researchers that need to conduct efficient and controlled clinical trials.
Oomnia, developed by Wemedoo, is a comprehensive, cloud-based SaaS platform that aims to revolutionize clinical trial management, particularly through its robust Electronic Data Capture (EDC) capabilities. Designed to streamline all aspects of clinical trials, Oomnia offers a unified platform that integrates multiple modules such as EDC, eSource, RTSM, eTMF, ePRO, eCOA, and CTMS, thereby reducing the need for separate systems and improving data flow across trial processes. This integrated approach is one of its most significant strengths, offering a seamless environment for data collection, management, and analysis. One of Oomnia’s standout features is its user-friendly interface, designed with simplicity and efficiency in mind. The platform utilizes drag-and-drop functionality, making it accessible even to those with no coding experience. This design choice lowers the learning curve, allowing users to quickly get up to speed. The ability to access the platform from any device and work offline further enhances usability, making it flexible and adaptable to the needs of clinical trial teams who often work in diverse environments.
Pros & Cons
- +All-in-one software solution with unified tools.
- +Real-time analytics and reporting.
- +Full interoperability with other systems.
- +High scalability for any trial type.
- +User-friendly interface with an easy learning curve.
- +Advanced data security with customizable access controls.
- +24/7 professional assistance and support.
- +Flexible customization options for workflows.
- +Significant time and cost savings.
- −Limited information on pricing.
- −Unclear specifics about integration with legacy systems.
- −Potential complexity for new users despite the user-friendly interface.
- −Limited details on performance metrics for large-scale trials.
Features
Key features
- Unified Platform
- Integrates EDC, eSource, RTSM, eTMF, ePRO, eCOA, eConsent, and CTMS into a single platform.
- Real-time Data and Analytics
- Provides immediate access to data and analytics across all tools and systems.
- Interoperability
- Fully interoperable with other systems, allowing for data import and export in various formats.
- User-Friendly Interface
- Designed for ease of use with drag-and-drop functionality and no coding required.
- Scalability
- Supports trials of any size, with unlimited patients, users, and sites.
- Data Security
- Employs robust security protocols to protect sensitive data.
- Professional Support
- Offers 24/7 professional assistance.
Additional features
- Comprehensive Clinical Trial Software
- An all-in-one solution covering various aspects of clinical trial management.
- SaaS Solution
- Offered as a Software-as-a-Service platform.
- Instant Data Quality
- Aims for near 100% data quality upon entry.
- Time Savings
- Claims to save more than 50% of the time in clinical trials.
- Cost Reduction
- Aims to reduce clinical trial costs by more than 50%.
- Unified EDC/eCRF
- Electronic Data Capture/Electronic Case Report Form functionality.
- eSource
- Electronic Source Data capture.
- RTSM
- Randomization and Trial Supply Management.
- eTMF
- Electronic Trial Master File.
- ePRO
- Electronic Patient-Reported Outcomes.
- eCOA
- Electronic Clinical Outcome Assessment.
- eConsent
- Electronic Informed Consent.
- CTMS
- Clinical Trial Management System.
- Adaptive Flexibility
- Adapts to different trial types and needs.
- Easy Learning Curve
- Designed for quick onboarding and user adoption.
- Instant Collaboration
- Facilitates real-time collaboration among team members.
- Swift Validation Process
- Streamlined validation processes.
- ISO 9001 and ISO 27001 Certified
- Adheres to quality management and information security standards.
- 24/7 Professional Assistance
- Provides round-the-clock support.
- Infinite Trial Types Supported
- Supports hybrid, decentralized, synthetic, real-world data, and medical device trials.
- Access From Everywhere
- Accessible from any location and device, with offline capabilities.
- Real-time Reporting
- Offers on-the-fly metrics and reporting.
- Infinite Trial Scalability
- Can handle an unlimited number of patients, users, and sites.
- Highest Data Security
- Employs robust security measures.
- Seamless Collaboration
- Facilitates real-time collaboration with audit logs.
- Insightful Analytics and Assets
- Provides access to a knowledge database and real-time metrics.
- Convenient Customization
- Allows for customization of documents and templates.
- Professional Trial Services
- Offers various services, including protocol development, data management, and medical writing.
- Medical Device Trials Support
- Specifically caters to medical device trials.
- Real-World Data Trials Support
- Supports trials using real-world data.
- Decentralized Trials Support
- Facilitates decentralized clinical trials.
- AI Features
- Integrates artificial intelligence capabilities
Pricing
Countries & Languages
Available in
Interface languages
Billing currencies
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About Oomnia
Oomnia is a clinical trial software/platform from Wemedoo that provides clinical trial tools. It combines eConsent, unification, and professional assistance so users can access a unified solution for their clinical trials. The platform supports interoperability and allows access from anywhere, making it easier to manage various phases of clinical research. Oomnia is designed to cater to the needs of clinical trial professionals, offering a comprehensive approach to data management and collaboration among teams. Key capabilities: eConsent Unification Professional Assistance Interoperability Access from Anywhere Best for: clinical researchers that need to conduct efficient and controlled clinical trials.
Oomnia Details
Oomnia's In-App Market Place
Does Oomnia have an in-app market place?
Yes
How many Mini-Apps in the marketplace?
1
Mini Apps
N/A
Pricing Options
Accepted Payment Currencies
USD ($), EUR (€), GBP (£), JPY (¥), AUD (A$), CAD (C$), CHF (CHF), CNY (¥), SEK (kr), NZD (NZ$), KRW (₩), INR (₹), RUB (₽), BRL (R$), MXN (Mex$), SGD (S$)
Pros & Cons
- All-in-one software solution with unified tools.
- Real-time analytics and reporting.
- Full interoperability with other systems.
- High scalability for any trial type.
- User-friendly interface with an easy learning curve.
- Advanced data security with customizable access controls.
- 24/7 professional assistance and support.
- Flexible customization options for workflows.
- Significant time and cost savings.
- Limited information on pricing.
- Unclear specifics about integration with legacy systems.
- Potential complexity for new users despite the user-friendly interface.
- Limited details on performance metrics for large-scale trials.
Oomnia's Support Options
Email Address
info@wemedoo.comContact
+41 41 740 0124Oomnia's Alternatives
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