The power you want,
the flexibility you need:
all in one clinical software suite

Clincase is designed for today’s clinical trials that are challenging, complex and must meet stakeholders’ needs and regulatory requirements. That’s why Clincase’s robust platform and high customizability are appreciated all around the world.

All-in-One Clinical
Software Suite

The Clincase suite offers a developer-centric programming interface. Alongside our intuitive tools for investigators and powerful capabilities for data managers and monitors, Clincase offers a comprehensive set of functionalities to collect, process, review, and report data, while also providing rich data visualization capabilities.

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EDC

Collect, manage, and store real-time clinical study data, ensure efficiency, and regulatory compliance

ePRO

User-friendly patient-centric ePRO solution facilitating submission of data

eCRF Design

User-friendly templates and easy creation and modification using a scripting language

Randomization & Trial Supply Management

Efficient medication supply and allocation with a versatile workflow

SAE Functionality

Delivers high efficiency and accuracy AE/SAE report

API Integration

Facilitates remote acquisition of data coming from wearable device, health app or CTMS

Data Visualization

Powerful and self-configurable reports and dashboards for informed decision-making

Alerts & Notifications

Delivers customizable content and conditions to trigger alerts to target audiences

Randomization

Seamless eCRF integration, unlimited stratification parameters, and block randomization

EDC

Collect, manage, and store real-time clinical study data, ensure efficiency, and regulatory compliance

ePRO

User-friendly patient-centric ePRO solution facilitating submission of data

eCRF Design

User-friendly templates and easy creation and modification using a scripting language

Randomization & Trial Supply Management

Efficient medication supply and allocation with a versatile workflow

SAE Functionality

Delivers high efficiency and accuracy AE/SAE report

API Integration

Facilitates remote acquisition of data coming from wearable device, health app or CTMS

Data Visualization

Powerful and self-configurable reports and dashboards for informed decision-making

Alerts & Notifications

Delivers customizable content and conditions to trigger alerts to target audiences

Randomization

Seamless eCRF integration, unlimited stratification parameters, and block randomization

Why Clincase

Build and Maintenance

  • Powerful eCRF design environment that supports trials with complex requirements
  • Automation, scripting, and APIs to empower Data Managers

Control

  • Metrics reporting for control of trial progress, efficiency and data quality
  • Full audit trail for all user actions in the system

Assure

  • Compliant with FDA 21 CFR Part 11, EU GMP Annex 11, ICH - GCP, and GDPR requirements
  • Comprehensive software validation package

Use

  • Easy-to-learn interface that both Investigators and participants will love
  • Works across browsers, smartphones, tablets, and desktop computers

Connect

  • ICH E2B, MEDDRA, WHODD encoding
  • API to synchronize with medical apps, CTMS, and wearable devices

Visualization

  • Preview of Data and Graphs
  • Visualize on-line study participant status

Innovative, Proven,
and Trusted Solution

SUBJECTS

STUDIES

COUNTRIES

Customers love
using Clincase

Rated 4.6/5 on G2.com

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Avatar of Hassan Kazerooni
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Avatar of Benoît Baron
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We are using Clincase as our preferred EDC system since 15+ years, this says it all. We have successfully implemented eCRFs in many clinical and non-interventional studies with Clincase. Due its outstanding flexibility and impressive functional capabilities Clincase has always proven to be the right solution whether it was a 10-year observational study or a very complex phase I/II oncology clinical trial. Clients have been particularly impressed by the ease of use, and the fully integrated modules for ePRO, randomization, drug supply and risk-based monitoring support.
Jens Knösel

Jens Knösel

Director eClinical Services

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LATEST

Clincase at ACDM25

ACDM 2025 Recap: Innovation, AI, and Reconnecting with the Data Management Community

The ACDM Conference 2025 in Prague, held from 2 to 4 March, brought together representatives from over 180 organizations in the clinical data management community to learn, share, and network. With a packed two-day program, pre-conference workshops, and insightful discussions, the event served as a hub for industry experts to explore the latest advancements in clinical data management. Featuring world-class speakers, hands-on workshops, and valuable networking opportunities, ACDM25 fostered meaningful discussions that are shaping the future of clinical trials.

International Womens Day 2025

Beyond Inclusion: Addressing Data Gaps in Women’s Healthcare

In recent years, clinical trials have made progress in improving gender representation, but inclusion alone is not enough. The real challenge lies in how data is captured, analyzed, and applied—ensuring that research accounts for the biological, hormonal, and metabolic differences between men and women. Without structured, meaningful data collection, critical insights are missed, and healthcare outcomes remain unequal.

EUCROF25 Home Trial Services Panel

Decentralized Trials Must Put Patients First—Not Just Technology

At EUCROF 2025 in Copenhagen, Monique Dugueperoux, our Business Development Manager, attended a panel discussion on home trial services, where key stakeholders—sponsors, patients, sites, CROs, and health authorities—shared insights on the future of decentralized clinical trials (DCTs).