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Medical technology & devices

Navigate the unique complexities of MedTech trials with ease with a highly configurable EDC system, built-in compliance, and dedicated support from product experts.

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How we power MedTech research

From usability testing to post-market surveillance, there’s a lot to keep track of in MedTech and device trials. Prelude offers unparalleled flexibility, simpler compliance, and industry-leading customer support to help you run smoother clinical trials from early phase to post-market surveillance.

01

The problem

Device trials can span multiple sites, often with different sub-protocols and documentation requirements.

Our solution

Unlock site-specific versioning, mid-study updates, and full audit trails for simpler workflows across every site.

02

The problem

Collecting patient consent before trials and capturing feedback during and after the trial can be inconsistent and time-consuming.

Our solution

Let participants update consent and submit feedback digitally at any time with intuitive eConsent and a convenient ePRO mobile app.

03

The problem

Supply chain issues and poor inventory visibility can delay device dispensing and trial timelines.

Our solution

Track real-time dispensing and inventory levels with Prelude’s built-in RTSM so you can make sure the right devices and medications are always on hand.

Powerful features for MedTech research

Don’t let your EDC add to the complexity of your MedTech research. Prelude was built to simplify complex workflows so you can focus on what matters most: your research.

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Site-specific protocol versioning

No more juggling multiple databases. Easily manage multiple protocol versions across sites with built-in compliance tools that log all changes and updates.

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Drag-and-drop form builder

Design forms your way so they work best for your trial — no coding experience required. Use cross-form edit checks and calculations to reduce errors and speed up validation.

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All-in-one capabilities

Save time with options for additional capabilities built directly into the EDC, like medical coding and site invoicing. Plus, leverage our API to connect to your existing tech stack.

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What our clients say about us

“Prelude makes collecting data easy for study sites and easy to review and analyze for the Sponsor.”

Alexandria C.

“Great experience for first time EDC builder. They were constantly helping us troubleshoot and ensuring what we built worked for all stakeholders. ”

Carly P. Field Trials Coordinator

“The software is very intuitive to use alongside a very user-friendly interface to build and develop data capture forms.”

Joe P. Research Coordinator

“This software provides all the functionality we need to collect high-quality veterinary clinical data. No two studies are the same, so the ability to quickly customize for each study is important.”

Kathy G. Worldwide Director Clinical Studies

“Prelude EDC is the best EDC software that I have used. The functionality gives the ability to provide customized CRF pages with visit structures that mimic the Protocol exactly.”

Margie Director of Biostatistics and DM

“Prelude EDC is a great user-friendly EDC on the frontend and backend.”

Meghana Data Manager

“Highly customizable forms can be made with the building tool, and the on-form calculations, conditional fields and error checks are very helpful to prevent data entry errors.”

Verified User Research

How we empower MedTech researchers

MedTech studies require that teams be fast, accurate, and adaptable. Prelude empowers your team with flexible form building, streamlined mid-study updates, and built-in tools that simplify compliance and data collection across every phase.

Customizable builder for complex protocols

Build studies that match your protocol without any coding. Use our drag-and-drop builder, advanced calculations, and cross-form edit checks to simplify your workflows and launch your medical device trials faster.

Built-in version control and audit trails

When protocols shift mid-study, you need to adapt while maintaining compliant data tracking. Prelude supports researchers with protocol amendment version controls and full audit logs so you always know what changed, when, and why.

Real-time supply tracking

Don’t spend your time stressing about inventory challenges. Track real-time patient dispensing and monitor inventory levels so you can make sure you always have the right supply on hand for your participants.

Remote-ready eConsent and ePRO

Make it easy for patients to sign informed consent and self-report from anywhere with intuitive eConsent and an ePRO mobile app. Media uploads and multilingual support improve the patient experience and boost engagement.

Related products and services

Prelude gives you everything you need to run smarter MedTech trials. Explore powerful solutions for seamless studies.

MedTech FAQs

Get answers to all of your MedTech questions.

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