At Prelude, we’re on a mission to build powerful tools that simplify clinical research. Our flexible, intuitive EDC platform is designed for complex studies and backed by real, personalized human support. The result? Enterprise results with a boutique feel.
Solutions designed for your study
Clinical trials are complicated. Your eClinical technology doesn’t have to be. Prelude cuts through the noise to power innovation and make life easier for research teams.
EDC
Build, launch, and manage complex studies with our flexible, no-code platform that makes clean data easier to capture and manage.
ePRO
Let participants report from anywhere with an intuitive mobile app that keeps participants engaged and data collection on track.
eConsent
Streamline informed consent with digital forms and clear, trackable workflows that simplify compliance and empower participants.
RTSM
Manage randomization and track trial supply in one seamless system, tailored to your protocol and designed to keep sites moving.
Our expertise
For over two decades, we’ve helped teams in 25+ countries and dozens of therapeutic areas run complex clinical trials. Our high-touch service and advanced customization options have powered thousands of studies, helping researchers innovate and bring new treatments to market faster.
Therapeutic areas
Oncology
Streamline oncology trials with advanced tools built to manage complex protocols and adaptive designs without the bloated cost.
Central nervous system (CNS)
Support CNS trials with highly configurable tech designed for longer timelines, complex protocols, and imaging stored directly in the EDC.
Rare disease
Improve recruitment and support adaptive protocols with better site experience and flexible technology.
Infectious diseases
Move quickly with tools designed to keep up with high-enrollment and fast-moving trials that need to launch fast.
Industries
Academia
Launch investigator-led studies faster with intuitive tools, flexible pricing, and built-in compliance.
Animal Health
Streamline companion and livestock research with an end-to-end platform built for a variety of species and regulatory needs.
Biotech & Pharmaceuticals
Run faster, leaner complex trials in global and multi-site studies with technology that flexes and scales with you.
Medical Technology & Devices
Support every phase of MedTech trials with built-in tools for device validation, regulatory tracking, and real-world evidence.
Discover the power of Prelude
Seamless data capture
Simplify data collection and keep sites happy with eCRFs that mimic the look and flow of paper forms.
Faster study builds
Build complex studies faster and easier than ever with drag-and-drop forms and no-code support for advanced calculations.
Adaptive by design
Manage cohorts and make mid-study updates without downtime or migrations — all while maintaining data integrity and compliance.
Easy patient participation
Gather reliable participant data from anywhere with an intuitive ePRO mobile app and automated reminders.
High-touch support
Onboard quickly with a dedicated product expert and hands-on training from our in-house team.
Cost-effective pricing
Unlock powerful enterprise-grade capabilities without the enterprise price tag.
Compliance you can count on
Prelude is fully compliant with 21 CFR Part 11, ICH GCP, GDPR, and Annex 11 so your trial data stays secure, documented, and ready for inspection.
What our clients say about us
“The only EDC that matters! From study build to database lock and study archiving... when you are in complete chaos... you can count on this NOT being on your list of frustrations”
Annie Consultant & Former Lead Monitor“Incredible EDC with unparalleled versatility and customizability! Everything you can possibly need to run a clinical trial is wrapped up in one package with customizability for the project at hand.”
Anonymous Program Administrator“It is a one-stop shop product for clinical trials management.”
Malathi Associate Scientist“Extremely easy to use and intuitive interface whether for Sponsor or Site side. Remarkable ability to control the presentation of DCFs. Easy to code on back end.”
Jacky M. Director Clinical Development