Healthcare & Medical Devices

Accelerated FDA & IEC 62304 Documentation
- Rapid generation of validated test scripts in natural language
- Comprehensive coverage of exploratory clinical and safety-critical scenarios
- Audit-ready documentation adhering to IEC 62304 and ISO 13485 standards
- Inspection-ready evidence packages for FDA, CE Mark, and certification bodies
Automated Regulatory Validation
- Generate audit-ready reports automatically with every test execution
- Maintain end-to-end traceability: requirement → test → execution → defect → resolution
- Live dashboards provide continuous visibility into compliance readiness and quality posture
Complete Clinical Workflow Coverage
- Patient intake, EMR documentation, prescription workflows, diagnostic orders, imaging systems
- Design clinical scenarios once, execute across dev, staging, and production environments
- Validate medication safety checks, clinical decision support, and alert mechanisms comprehensively
HIPAA-Grade Data Protection
- Intelligent automatic masking of PHI: patient identities, MRNs, SSNs, clinical details, treatment histories
- Built-in audit trails satisfy regulatory inspection requirements
- All test artifacts maintain complete data privacy and security standards
High-Scale Safety-Critical Regression
- Execute complete safety-critical regression suites with every build
- Parallel execution across multiple environments using distributed remote agents
- Self-healing tests require negligible maintenance despite frequent UI changes
- Free your team to focus on exploratory testing and edge-case scenario validation
Subscribe today.
Be the first to hear about our latest
news and updates
Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.


