Prelude EDC logo

Prelude EDC

by Prelude · Since 2003
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ActiveAvailable globallyCloud
Quick facts
VendorPrelude
Year launched2003
StatusActive
Location5725 Highway 290 W, Suite 201 , Austin, Texas 78735, US
Countries servedGlobal
Languages6
Integrations
Free tier
Free trial
Contact salesYES

About Prelude EDC

Prelude EDC is an electronic data capture software from Prelude that supports clinical trial processes. It provides flexible study designs, compliant data management, and customer support at every stage so researchers can execute complex trials more efficiently. Prelude EDC allows teams to build studies quickly while ensuring data integrity and compliance with regulatory standards. The platform is designed to simplify the complexities of research, offering tools tailored to specific study needs. Key capabilities: flexible study design compliant data management reliable reporting tools user-friendly interface extensive customer support Best for: clinical researchers that need efficient data capture for complex trials.

Prelude EDC is a cloud-based electronic data capture (EDC) software designed to streamline data collection and management for clinical trials. It offers a flexible, user-friendly platform that supports clinical researchers, trial coordinators, and investigators in managing and capturing trial data efficiently and accurately. The primary goal of Prelude EDC is to simplify the complexities of clinical trials by enabling seamless data entry, validation, and real-time data access. Key features include customizable electronic case report forms (eCRFs), data validation checks, monitoring tools, and real-time reporting capabilities, all aimed at improving data quality and reducing time spent on administrative tasks. The user interface of Prelude EDC is clean, intuitive, and easy to navigate. The design emphasizes simplicity while maintaining functionality, making it suitable for both new users and experienced clinical professionals. The interface is organized with a well-structured layout, where users can easily find essential features such as form entry, data review, and real-time data analysis. Customizable dashboards provide quick access to key study metrics, and the navigation system is straightforward, reducing the learning curve typically associated with complex clinical trial software.

Pros & Cons

What users like
  • +User-friendly: Intuitive interface, mimics paper forms, easy to learn.
  • +Highly customizable: Tailored to specific study needs, even complex designs.
  • +Excellent support: Dedicated Customer Success Managers provide personalized help.
  • +Comprehensive platform: Supports preclinical to post-market studies, includes ePRO.
What users flag
  • Calculations can be complex: Requires some learning, though training is available.
  • Potential for untested revisions: A possible issue to watch out for.

Features

Key features

User-Friendly Interface
Designed to mimic paper forms for easy data entry, aiming to be intuitive and require a low learning curve. Emphasis on investigator preference.
Customizable Design
Flexible study builder allows tailoring forms to specific study needs, including complex designs and preclinical studies.
End-to-End Platform
Supports preclinical to post-market studies, covering the entire clinical data management process.
ePRO Mobile App
Enables direct patient data input, improving data collection frequency and compliance.
Dedicated Customer Success Managers
Provides personalized support from training to study build and maintenance, acting as an extension of the client's team.
Affordable Pricing
Offers comparable flexibility to high-end systems like Medidata Rave but at a more standard EDC price point.
Regulatory Compliance
Adheres to 21 CFR Part 11, Annex 11, ICH GCP, and GDPR guidelines.
Wide Range of Therapeutic Areas
Experience across various therapeutic areas, from allergies to urology.
Comprehensive Support
Industry-leading onboarding and ongoing support from trained CSMs.

Additional features

Electronic Data Capture (EDC)
Web-based application for compliant clinical trial data collection.
Electronic Patient-Reported Outcomes (ePRO)
Mobile app for direct patient data input.
Professional Services
Customer Success Managers provide personalized support.
Customizable eCRF Design
Forms can be tailored to specific study requirements.
Study Builder
Robust tool for creating and managing studies.
Data Collection
Seamless data collection process.
Regulatory Compliance
21 CFR Part 11, Annex 11, ICH GCP, and GDPR compliant.
User-Friendly Workflows
Easy to build and manage.
Edit Checks and Calculations
Built-in tools to improve data quality.
Investigator-Preferred EDC
Designed with investigator input for ease of use.
Direct Patient Data Collection
ePRO app facilitates direct patient input and reminders.
Affordable Rate
Competitive pricing compared to high-end systems.
Industry-Leading Support
Dedicated CSMs provide comprehensive assistance.
Vast Background in Therapeutic Areas
Experience across a wide range of therapeutic areas.
Training
Hands-on training provided by CSMs.
Study Build and Maintenance
CSMs can assist with or manage these processes.
Real-time data access (implied)
Mention of "one database for everything" suggests real-time data visibility.
Query notifications
System sends notifications of queries.
Single database system
Regulatory, EDC, and invoicing information are all stored in one place.

Pricing

Free trial
Free version
Request a quote
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Countries & Languages

Global
Countries served
6
Interface languages
15
Billing currencies

Interface languages

EnglishFrenchGermanSpanishJapaneseChinese

Billing currencies

🇺🇸USD🇪🇺EUR🇬🇧GBP🇯🇵JPY🇦🇺AUD🇨🇦CAD🇨🇭CHF🇨🇳CNY🇸🇪SEK🇳🇴NOK🇩🇰DKK🇰🇷KRW🇮🇳INR🇷🇺RUB🇧🇷BRL

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