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
IntegrationsN/A
Free tierN/A
Free trialN/A
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

Pros
  • 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.
Cons
  • 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
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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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