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.
Medrio EDC
Medrio EDC is a clinical data management solution that helps you capture, manage, and report clinical trial data through a secure, cloud-based interface to accelerate your study timelines.
Quick Comparison
| Feature | ClinCapture | Medrio EDC |
|---|---|---|
| Website | clincapture.com | medrio.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 | 2005 |
| Headquarters | San Jose, USA | San Francisco, 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.
Medrio EDC
Medrio EDC provides you with a flexible environment to manage clinical trials of any phase or complexity. You can build your studies in days rather than months using an intuitive interface that requires no programming knowledge. This allows your team to focus on data quality and patient safety instead of wrestling with complex technical setups. By centralizing your clinical data, you gain real-time visibility into study progress and site performance.
The platform is designed for pharmaceutical companies, biotech firms, and CROs who need to streamline their data collection processes. You can easily manage mid-study changes, perform complex validation checks, and ensure regulatory compliance with built-in audit trails. Whether you are running a small Phase I study or a large multi-center global trial, the software scales to meet your specific data management requirements while reducing manual entry errors.
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.
Medrio EDC Features
- Drag-and-Drop Study Builder. Build your clinical databases and forms visually without writing a single line of code to get your study started faster.
- Mid-Study Changes. Apply updates to your live study forms and logic instantly without needing to take your entire system offline.
- Offline Data Entry. Capture critical patient data even when you lack an internet connection and sync it automatically once you are back online.
- Real-Time Edit Checks. Set up automated validation rules that flag inconsistent data immediately, ensuring higher data quality at the point of entry.
- Medical Coding. Streamline your coding process with integrated dictionaries like MedDRA and WHODrug to maintain consistent terminology across your trial.
- E-Source Integration. Eliminate redundant data entry by capturing information directly from patients or sites and syncing it directly into your EDC.
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
Medrio 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
Medrio EDC
Pros
- Extremely fast study build times compared to legacy systems
- Intuitive interface requires very little training for site staff
- Excellent customer support with rapid response times
- Easy to implement mid-study changes without downtime
Cons
- Reporting tools can be difficult to master initially
- Customization options for complex exports are sometimes limited
- Pricing can be high for very small Phase I studies