Easy to use
Powerful
Affordable
DISTILL EDC is built from the ground up to put you in control. Experience agility that makes an impact on your study, not on your budget.
Simpler, Smarter EDC for Small-Budget CROs, Biotechs, and University Trials.
Whether you're a CRO, biotech startup, or university research team, managing data shouldn’t feel like a full-time job. DISTILL EDC system is designed for smaller budgets and lean teams, providing powerful data collection tools that scale as you grow — without the hefty costs of traditional systems.
No More Spreadsheets. No More Chaos. Just Simple, Powerful Data Collection.
Tired of juggling spreadsheets and manual entries? DISTILL EDC platform replaces disconnected tools with a unified system for data collection, tracking, and analysis — all in one clean, user-friendly interface. Say goodbye to errors, delays, and data chaos.
Empower Your Data Managers - Self-Design and Publish Without Specialist Programmers.
Why wait for programmers to design your clinical study forms? Our no-code EDC solution empowers your data managers to create, customize, and publish workflows instantly. Gain total control over your trials and make adjustments in real-time without technical support.
Your Data, Your Way - Take Control of Every Trial with Intuitive EDC Tools.
Every research project is unique — your EDC system should be too. With self-customizable forms, real-time analytics, and seamless collaboration, DISTILL EDC gives you the control to run your trials the way you want. No rigid templates. No limits.
Key Features at a Glance
Get a quick look at the core functionalities that make DISTILL EDC system simple, powerful, and intuitive. From custom form design to regulatory compliance, these essential features ensure you have everything you need to run successful clinical trials — all in one place.
Custom Form Builder
Real-Time Data Collection
Intuitive Workflow Designer
Data Validation Rules
Role-Based Access Control
Audit Trail &
Change Logs
eSignatures & Approvals
GDPR, HIPAA, 21 CFR Part 11
Custom Reports & Exports
Multi-Language Support
Offline Data Entry
Real-Time Alerts & Notifications
Data Security & Encryption
Automated Queries & Issue Tracking
Multi-Device Compatibility
Dashboards & Visualizations
File Attachments
Customizable Branding
Bulk Data Uploads
Randomisation
Who we are
Here’s the team that makes it all happen. From developers and DevOps engineers to testers, scrum masters, business analysts, and business development executives, each person here plays a vital role in bringing our EDC system to life. Our shared goal is simple: to build a platform that’s intuitive, powerful, and truly useful for our users. Together, we’re driven by a passion for innovation, collaboration, and customer success.
Anthony Damian
Managing Director
Jean-Pascal Rugiero
Vice President
Sachin Adiseshadrirao
Operations Manager
Suvajit Swapan Jhuri
Client and Project Manager
OCT China | 03 Sep to 04 Sep | Suzhou, China
CRO Summit Europe | 16 Sep to 17 Sep | Amsterdam
OCT Southern Cal | 23 Sep to 24 Sep | San Diego, USA
SCDM Global | 27 Sep to 30 Sep | Baltimore, USA
Scope Europe | 14 Oct to 15 Oct | Barcelona, Spain
OCT New England | 15 Oct to 16 Oct | Boston, USA
DIA Japan | 19 Oct to 21 Oct | Tokyo, Japan
Clinical Trials 17 | 12 Nov to 14 Nov | Shanghai, China
COG Europe | 18 Nov to 19 Nov | Amsterdam
OCT East Asia | 02 Dec to 03 Dec | Seoul
SCDM India | 12 Dec to 13 Dec | Hydrebad, India
See You at These Upcoming Conferences
We believe that the best connections happen face-to-face. That’s why we’re hitting the road and attending key industry conferences. It’s a chance for us to meet you, learn from you, and showcase how DISTILL EDC can transform your clinical trials. Check out the upcoming events where you can find us — we’d love to connect, answer your questions, and show you what DISTILL EDC system can do.
Ensuring Regulatory Compliance with DISTILL: GCP, 21 CFR Part 11, and Beyond
In the evolving landscape of clinical research, regulatory compliance is not just a requirement; it is the foundation of trust, patient safety, and data integrity. With increasing trial complexity, decentralized models, and the integration of digital health tools, ensuring adherence to Good Clinical Practice (GCP), 21 CFR Part 11, and global data protection frameworks like GDPR is more critical than ever.
This whitepaper explores how modern Electronic Data Capture (EDC) platforms embed compliance into every workflow, ensuring trials are both agile and compliant.