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.
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.
Learn MoreSUBJECTS
STUDIES
COUNTRIES
Rated 4.6/5 on G2.com
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
Director eClinical Services
We're on the pulse of industry developments and respond pro-actively to the needs of our customers.
LATEST
-min.webp&w=1200&q=75)
Clincase EDC Implementation: Supporting Real-World Study Workflows
Clincase’s hybrid methodology brings structure and flexibility to every EDC implementation. In this article, our Implementation Manager, Caroline Chong, and her team walk through how that approach takes shape in real-world studies — from understanding complex protocols to delivering tailored system configurations.
How Clincase’s Hybrid Methodology Keeps EDC Implementation Agile, Focused, and On Track
Every successful clinical trial starts with a team that knows how to turn complex protocols into working systems. At Clincase, we use a hybrid project management methodology that blends structure and flexibility to guide EDC implementation from planning through go-live. In this article, developed with our Implementation Manager, Caroline Chong, we explain how her team supports sponsors and CROs by delivering setups that align with operational workflows and meet regulatory requirements.
Why Choosing the Right EDC System Is Critical for Clinical Trial Success
Clinical trials are growing more complex — not just scientifically, but operationally. As protocols evolve and timelines tighten, mid-sized CROs must deliver faster, more tailored trials with leaner teams. Choosing the right EDC system is critical to keeping pace and staying competitive.