🇨🇭 Swiss Precision & Compliance

Unified Clinical Trial Software

Clinical trial software across therapeutic areas

oomnia supports clinical research teams working across different therapeutic areas, helping address complex clinical challenges through unified clinical trial software

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21 CFR Part 11 ICH-GCP GDPR GxP-aligned

Therapeutic Areas

A therapeutic-area agnostic clinical trial platform

oomnia is designed to support different therapeutic areas, unifying essential tools teams need to support therapy‑specific research

Cardiovascular, renal, and metabolic diseases

Designed for large-scale, longitudinal, and event driven studies

Dermatology

Supporting the evaluation of new and innovative dermatology treatment options

Endocrinology

Precise management of long term metabolic, hormonal, and biomarker data

Gastroenterology

Helping manage complex gastroenterology trials from study start up through completion

Hematology

Built for highly variable diseases and evolving treatment approaches

Immunology and inflammatory diseases

Helping teams track highly variable biomarkers and symptoms

Infectious diseases

Unifies clinical operations for fast moving, data intensive trials

Neurology

Longitudinal data tracking and clearer visibility into disease activity and treatment effects

Oncology

Supports adaptive, data intensive oncology trials

Ophthalmology

Imaging, clinical, and patient reported data fully aligned

Rare and orphan diseases

Enabling teams to manage small, globally distributed patient populations

Respiratory diseases

Connects all key stakeholders involved in respiratory clinical trials

Who We Work With

Designed for every clinical research team

oomnia supports a wide range of clinical research teams by adapting to different study types, organizational sizes, and operational needs. Whether supporting large, global programs or academic institutions, oomnia delivers the flexibility, structure, and insight needed to keep studies moving efficiently.

Explore how oomnia supports different organizations

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.

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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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Clinical Trial Types

Supporting all clinical trial types across therapeutic areas

oomnia is designed to support a wide range of clinical trial types within a single platform, removing the need to manage different systems for different study models.

With a unified architecture and configurable workflows, research teams can run interventional, decentralized, real world, and hybrid trials while maintaining consistent processes, reliable data handling, and centralized oversight across studies.

Explore how oomnia supports different clinical trial types

Get Started

See how oomnia adapts to your therapeutic research needs

See how oomnia’s unified environment can simplify your clinical trial execution and keep teams aligned in real time

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Frequently asked questions (FAQ)

What therapeutic areas does oomnia support?

oomnia supports a wide range of therapeutic areas, including oncology, hematology, endocrinology, neurology, cardiovascular and metabolic diseases, rare and orphan diseases, immunology, dermatology, infectious diseases, respiratory diseases, ophthalmology, and gastroenterology.

Can oomnia support therapeutic areas not listed on this page?

Yes. oomnia is built to support additional therapeutic areas beyond those listed, adapting workflows, data capture, and study configurations to meet the needs of new or emerging research areas.

How does oomnia adapt to therapy‑specific research requirements?

oomnia allows teams to configure workflows, data structures, and study processes to align with therapy‑specific protocols, endpoints, and data types, while keeping everything within a unified clinical research information system.

Is oomnia suitable for complex and data‑intensive therapeutic areas like oncology or neurology?

Yes. oomnia is designed to handle adaptive trial designs, longitudinal data tracking, biomarker‑heavy datasets, and complex endpoints commonly required in oncology, neurology, and other data‑intensive therapeutic areas.

How does oomnia support rare and orphan disease research?

oomnia supports rare and orphan disease studies by enabling management of small, globally distributed patient populations, flexible data capture, and centralized oversight across sites and regions.

Can oomnia manage different types of data across therapeutic areas?

Yes. oomnia supports a broad range of data types, including clinical data, patient‑reported outcomes, biomarker data, imaging data, and longitudinal follow‑up data, depending on the therapeutic area and study design.

Can workflows be standardized while still supporting different therapeutic needs?

Yes. oomnia unifies core clinical workflows in one platform while allowing therapy‑specific customization, enabling consistency across studies without limiting flexibility.

Does oomnia scale across multiple therapeutic areas within the same organization?

Yes. oomnia is designed to scale across departments and research programs, allowing organizations to run studies in multiple therapeutic areas simultaneously using a single, unified platform.

How does oomnia support regulatory requirements across different therapeutic areas?

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