Formedix ryze
Clinical trial automation software and services.
Overview
Formedix ryze is an eClinical platform that differentiates itself by focusing on the automation of clinical trial study builds. It is a metadata-driven platform that helps sponsors and CROs design, build, and manage clinical studies based on CDISC standards. While it includes EDC, eCRF, and ePRO capabilities, its core strength lies in creating reusable assets and automating the process of building study databases, which significantly speeds up trial startup.
✨ Key Features
- Metadata repository (MDR) for study asset reuse
- Automated study build from standardized metadata
- CDISC standards compliance (SDTM, CDASH, Define-XML)
- Integrated EDC, eCRF, and ePRO design
- Visual, drag-and-drop study design interface
🎯 Key Differentiators
- End-to-end automation of the study build process based on a metadata repository
- Strong focus on CDISC standards and asset reuse
- Vendor-agnostic, can be used to build studies for different major EDC systems
Unique Value: Dramatically reduces clinical trial build times and costs by enabling the creation and reuse of standardized, compliant study assets.
🎯 Use Cases (4)
✅ Best For
- Used by pharmaceutical companies to streamline their end-to-end study setup processes and ensure standards compliance.
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Single, one-off studies with no need for standardization or asset reuse.
- Organizations not using or planning to use CDISC standards.
🏆 Alternatives
Instead of building each study from scratch within an EDC system, Formedix allows you to design and automate the build process externally in a standardized way, leading to significant efficiency gains across a portfolio of trials.
💻 Platforms
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Phone Support
- ✓ Dedicated Support (Enterprise tier)
🔒 Compliance & Security
💰 Pricing
✓ 14-day free trial
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