Infinite Scalability Scale your clinical trials effortlessly with dynamic adaptability
Infinite Scalability Scale your clinical trials effortlessly with dynamic adaptability
Flexible Scalability for Any Trial
oomnia offers infinite scalability, empowering you to manage trials of any size, complexity, or scope with ease. Whether managing a small exploratory study, or overseeing a multinational clinical trial or a number of portfolios, oomnia provides the flexibility to adapt to your study’s changing needs.
By offering customizable workflows, reusable elements, and efficient data management tools, oomnia ensures that you can easily and efficiently scale your research infrastructure without compromising performance or accuracy.
Effortlessly Scale Trials to Meet Evolving Research Demands
Empower Your Research with Unlimited Scalability
Realize the full potential of your clinical trials, no matter the size.
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Expand your research capacity with seamless trial scalability.
oomnia enables effortless scalability with features designed to adapt to both small and large-scale clinical trials. From flexible configurations to professional support, oomnia ensures that your trial operations remain smooth and efficient, regardless of scale.
Effortlessly adjust to trials of any size or complexity.
As your trials and their numbers grow, oomnia instantly and automatically scales with you. Our software allows you to increase the number of trials, organizations, sites, and participants without any additional work or technical constraints. oomnia is fundamentally a multi-tenant system, with multiple trials on a single instance, thus enabling instant scalability in any manner that is necessary.
Increase the capacity for additional trials of any size, type, location, participants, or tools, seamlessly and without delays.
Our Proof of Quality
We are ISO 9001 and ISO 27001 certified. Our commitment to robust information security & superior quality management is at the core of our innovative solutions, ensuring reliable & efficient trial management for our clients.
Collect and integrate data effortlessly from diverse sources.
Efficient data management is key to trial success, especially when dealing with multiple trial sites. The oomnia data integration capabilities allow seamless synchronization of trial data from various sites ensuring that all stakeholders have access to real-time updates, and that trial information remains consistent across the board.
Automatically access data from all trials, their documents, and data sources, regardless of type, using oomnia EDC. Ensure real‑time aggregation, analysis, transparency, consistency, and updates.
Automate and optimize processes to handle growing complexity.
As your clinical trials scale, managing workflows can become increasingly complex. With the adaptable workflow of oomnia automation tools, you can efficiently manage larger datasets, participant numbers, and trial activities by automating key processes. This ensures that you can scale your trials on schedule, without the added burden of manual operations.
Adjust workflows automatically to manage more trials, documents, and increased participant numbers, regardless of where they are.
oomnia - Meeting Industry Standards
Our unified clinical trial software is designed with compliance at its core, meeting critical industry standards. Our commitment to these regulations ensures that your clinical trials are not only efficient but also adhere to the highest levels of data integrity, privacy, and ethical conduct.
21 CFR
PART11
compliant
HIPAA
compliant
GDPR
compliant
ICH GCP
compliant
SWISS DATA PRIVACY LAW
compliant
FAIR ALCOA+
compliant
Infinite scalability with oomnia empowers your clinical research teams to expand operations without limits. By providing seamless adaptability to any number of trials, regardless of their size or complexity, your teams can focus on groundbreaking research without worrying about technical constraints. With built-in flexibility and professional support, you can confidently scale your trials, ensuring smooth operations, increased efficiency, and optimized outcomes.
Seamlessly grow your research infrastructure to accommodate any number of trials of any type, size, or scope.
Scale your operations by streamlining trial workflows and reducing time spent on administrative tasks, freeing up resources for core research activities.
Benefit from expert technical assistance, ensuring smooth trial operations and minimizing disruptions.
