ClinCapture
ClinCapture provides a cloud-based electronic data capture platform that helps clinical researchers manage trials, collect patient data, and maintain regulatory compliance through a flexible, DIY software environment.
Medidata Rave EDC
Medidata Rave EDC is a clinical data management platform that captures and manages patient data for global clinical trials while ensuring regulatory compliance and data integrity.
Quick Comparison
| Feature | ClinCapture | Medidata Rave EDC |
|---|---|---|
| Website | clincapture.com | medidata.com |
| Pricing Model | Freemium | Custom |
| Starting Price | Free | Custom Pricing |
| FREE Trial | ✘ No free trial | ✘ No free trial |
| Free Plan | ✓ Has free plan | ✘ No free plan |
| Product Demo | ✓ Request demo here | ✓ Request demo here |
| Deployment | ||
| Integrations | ||
| Target Users | ||
| Target Industries | ||
| Customer Count | 0 | 0 |
| Founded Year | 2010 | 1999 |
| Headquarters | San Jose, USA | New York, USA |
Overview
ClinCapture
ClinCapture is a specialized electronic data capture platform designed to help you manage clinical trials with greater speed and lower costs. Instead of relying on expensive programming teams, you can use its self-service tools to build your own studies, design electronic case report forms, and manage complex clinical workflows directly from your browser.
You can streamline your entire data collection process while staying compliant with strict FDA and HIPAA standards. The platform is particularly effective for medical device companies and CROs who need to launch trials quickly without sacrificing data integrity or security. It offers a scalable environment that grows with your study requirements, from early-phase trials to large-scale global deployments.
Medidata Rave EDC
Medidata Rave EDC serves as the central hub for your clinical trial data, allowing you to capture, manage, and report on patient information with high precision. You can streamline the entire data entry process for site coordinators while maintaining strict adherence to global regulatory standards. The platform eliminates manual paper-based tracking by providing a unified environment where clinical teams can monitor study progress and data quality in real-time.
You can scale your research from small Phase I studies to massive global Phase III trials without switching systems. The software helps you reduce study build times and improve data visibility across your entire research portfolio. It is primarily used by pharmaceutical companies, contract research organizations (CROs), and medical device manufacturers who need a secure, validated environment for complex clinical research data.
Overview
ClinCapture Features
- Build Your Own Study Create and modify your clinical trials quickly using self-service tools without needing advanced programming or IT support.
- eSource Integration Capture patient data directly at the source to eliminate manual transcription errors and speed up your monitoring process.
- Electronic Signatures Maintain full regulatory compliance with built-in 21 CFR Part 11 signatures for investigators and site staff.
- Medical Coding Standardize your clinical data automatically using integrated MedDRA and WHODrug dictionaries for consistent reporting.
- Randomization Tools Manage subject assignments and drug kits directly within the platform to ensure study blinding and integrity.
- Real-Time Reporting Monitor your trial progress instantly with visual dashboards that track enrollment, queries, and data completion rates.
Medidata Rave EDC Features
- Unified Data Capture. Capture all your clinical trial data in one place to eliminate silos and ensure a single source of truth.
- Real-time Data Validation. Identify and resolve data discrepancies immediately with automated edit checks that fire as soon as you enter information.
- Flexible Study Build. Build your electronic case report forms once and reuse them across multiple studies to accelerate your trial timelines.
- Medical Coding. Code your adverse events and medications quickly using integrated dictionaries like MedDRA and WHODrug for consistent reporting.
- Targeted SDV. Reduce your monitoring workload by focusing Source Data Verification only on the most critical data points and high-risk sites.
- Global Library Management. Standardize your data collection across all global sites by managing a central library of validated forms and folders.
Pricing Comparison
ClinCapture Pricing
- Basic EDC capabilities
- Limited user seats
- Standard CRF templates
- Online support access
- Basic data export
- Everything in Free, plus:
- Unlimited data entries
- Advanced edit checks
- Medical coding modules
- Randomization (IWRS)
- Priority technical support
Medidata Rave EDC Pricing
Pros & Cons
ClinCapture
Pros
- Fast study setup compared to traditional EDC systems
- User-friendly interface for site coordinators and investigators
- Cost-effective for small to mid-sized medical device trials
- Excellent customer support during the study build phase
Cons
- Advanced reporting can be difficult to customize
- Learning curve for complex conditional logic builds
- Occasional lag during high-volume data exports
Medidata Rave EDC
Pros
- Highly scalable for large global clinical trials
- Gold standard for regulatory compliance and security
- Extensive integration with other Medidata clinical products
- Robust reporting capabilities for monitoring study progress
Cons
- Requires specialized training for study builders
- Initial setup and configuration can be time-consuming
- Higher price point compared to basic EDC tools