Is oomnia suitable for CROs and multi‑sponsor environments?

Yes. oomnia replaces fragmented vendor stacks with a single unified platform, helping CROs manage multiple sponsors, studies, and workflows while maintaining transparency, consistency, and operational control.

🇨🇭 Swiss Precision & Compliance

Unified Clinical Trial Software

Clinical trial software for healthcare and life science organizations

oomnia is a clinical trial software designed for biopharma companies, CROs, MedTech organizations, and research institutions, supporting diverse clinical trial models through unified data, workflows, and systems.

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21 CFR Part 11 ICH-GCP GDPR GxP-aligned

Who We Work With

Clinical trial platform for sponsors, CROs, and research organizations

oomnia is a clinical trial platform designed for healthcare and life science organizations of different sizes and structures.

It supports sponsors, CROs, MedTech companies, and research institutions by unifying clinical data, and workflow into a single, scalable environment.

Large biopharma

Manage complex global study portfolios with centralized oversight, standardized data, and consistent workflows across regions and programs.

Emerging and mid-sized biopharma

Scale clinical operations with flexible, configurable workflows and data structures that evolve as pipelines grow.

MedTech

Coordinate device-driven studies with unified data capture, faster study cycles, and improved operational visibility.

Academia

Streamline clinical research workflows and data management for teams operating with limited resources and infrastructure.

CROs

Replace fragmented vendor stacks with a unified clinical trial platform that improves coordination, data consistency, and delivery timelines across sponsors and studies.

Clinical trial units

Unify data, workflows, and teams across sites and departments within a centralized system.

Cosmetics

Manage cosmetic testing and safety documentation with unified workflows, reliable data control, and market-specific traceability.

Animal health

Run veterinary research and development on one clinical trial platform with visibility across species and regions.

Food industry

Streamline product development, quality assurance, and regulatory compliance with unified data management and end-to-end traceability across the food production lifecycle.

Nutraceuticals

Accelerate formulation, testing, and compliance with an integrated platform that ensures data integrity, supports health claims validation, and enables global market readiness.

Trial Types

One platform for every clinical trial type

oomnia supports a wide range of clinical trial models while maintaining consistent data structures and operational workflows.

Phase I–IV clinical trials Decentralized and hybrid trials Real-world data and observational studies

See how oomnia supports different clinical trial models →

Trusted partners

Global network of partners

oomnia Platform

Built to replace modular eClinical systems

oomnia unifies core clinical trial tools within a single platform to support diverse scientific and operational needs

EDC

Electronic Data Capture (EDC) Software

Streamline clinical data collection with our intelligent, compliant EDC system. Build complex trial designs quickly, reduce data entry errors, and ensure absolute data integrity.

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CTMS

Clinical Trial Management System (CTMS)

Gain complete, real-time oversight of your trial operations. Centralize site monitoring, track financial milestones, and manage your clinical teams from one unified dashboard.

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ETMF

Electronic Trial Master File (eTMF)

Maintain constant inspection readiness and compliance. Streamline your clinical document management with a secure, centralized repository that simplifies audits and tracking.

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RTSM

Randomization & Trial Supply Management (RTSM)

Automate complex patient randomization and optimize your clinical supply chain. Ensure the right treatments reach the right global sites exactly when they are needed.

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ECONSENT

Electronic Informed Consent (eConsent)

Improve patient comprehension and trial retention with an interactive, fully compliant digital consent experience that works seamlessly across devices.

Explore oomnia eConsent

EPRO

Electronic Patient-Reported Outcomes (ePRO)

Capture high-quality, real-time data directly from patients. Our user-friendly ePRO boosts patient engagement and compliance by making data submission effortless.

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ECOA

Electronic Clinical Outcome Assessments (eCOA)

Standardize your clinical assessments to ensure high-fidelity data collection. Eliminate paper-based inconsistencies and capture reliable outcome data across all global trial sites.

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ESOURCE

eSource Data Capture

Accelerate data availability by capturing clinical information directly at the point of care. Eliminate manual transcription errors and streamline source data verification (SDV).

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Therapeutic Areas

A therapeutic area-agnostic clinical trial software

oomnia is designed as a therapeutic area-agnostic clinical trial software, supporting studies across diverse indications while still addressing the unique operational, data, and regulatory challenges of each therapeutic area.

By using a unified data model and configurable workflows, teams can run studies in different therapeutic areas while maintaining consistent data structures, processes, and oversight.

See how oomnia supports research across therapeutic areas

Get Started

Discover how oomnia can support your clinical trials

Whether you are running early-phase studies, decentralized trials, or global multi-study programs, oomnia adapts to your needs.

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Frequently asked questions (FAQ)

What types of organizations use oomnia?

oomnia is used by large, emerging and mid-sized biopharma, CROs, MedTech organizations, academic institutions, clinical trial units, food industries, animal health, nutraceuticals, and cosmetics teams to manage clinical trials within a unified platform.

Can oomnia support organizations that are not listed on this page?

Yes. oomnia is designed to support many different types of organizations, even if their structure, scale, or study models differ from current client examples.

How does oomnia support both large and growing organizations?

oomnia scales to meet the needs of different organizations by providing flexible workflows, configurable tools, and a unified platform that can support both global, multi‑study portfolios and smaller, resource‑constrained teams.

How does oomnia support MedTech companies and device‑based studies?

oomnia helps MedTech teams coordinate device studies with faster development cycles by unifying data capture, oversight, and study workflows in one system, enabling clearer visibility across the trial lifecycle.

Can academic and clinical trial units use oomnia with limited resources?

Yes. oomnia is built to support academic teams and clinical trial units by streamlining workflows, reducing operational complexity, and enabling teams to manage studies efficiently without requiring extensive internal infrastructure.

How does oomnia adapt to different therapeutic areas across clients?

oomnia unifies eight clinical tools together in one system that can be configured to support different therapeutic areas, allowing clients to run diverse studies while maintaining consistent workflows and data practices.

Can oomnia support different clinical trial types?

Yes. oomnia supports Phase I–IV trials, decentralized and hybrid models, and real-world data studies, all within a single clinical trial software environment.

How does oomnia support regulatory compliance for different client types?

oomnia is built with regulatory readiness at its core, providing 21 CFR Part 11–ready records with full audit trails and secure electronic signatures, embedding Risk‑Based Quality Management aligned with ICH E6(R3) into routine workflows, and using CDISC‑aligned standards such as CDASH and SDTM‑compatible outputs, while supporting submissions across FDA, EMA, and other global health authorities.

Can oomnia replace multiple clinical trial systems?

Yes. oomnia unifies core clinical trial tools, including EDC, CTMS, RTSM, eTMF, ePRO/eCOA, eSource, and eConsent, reducing system fragmentation and improving workflow efficiency.