Design Verification is pruebas y evidencia que confirman que las salidas de diseño cumplen con las entradas de diseño mediante pruebas y análisis objetivos.
Complete Guide to Design Verification
Design Verification is a critical element of FDA Design Controls (21 CFR 820.30) that confirms design outputs meet the design inputs specified at the beginning of development. It answers the question: "Did we build it right?"
Design Verification vs Design Validation:
- Verification - Building it RIGHT (outputs meet inputs)
- Validation - Building the right thing (device meets user needs)
Purpose of Design Verification:
- Confirms design outputs satisfy design inputs
- Provides objective evidence through testing
- Ensures specifications are met before validation
- Identifies design flaws before manufacturing
Common verification activities:
1. Performance Testing
- Electrical safety testing
- Mechanical strength testing
- Software functionality testing
- Biocompatibility testing
2. Environmental Testing
- Temperature/humidity cycling
- Shock and vibration testing
- Transportation simulation
- Accelerated aging
3. Standards Compliance
- IEC 60601 electrical safety
- ISO 10993 biocompatibility
- ISO 14971 risk management
- Product-specific standards
4. Software Verification
- Unit testing
- Integration testing
- Code reviews
- Requirements traceability
Verification documentation:
- Verification Protocol - Test objectives, methods, acceptance criteria
- Test Reports - Detailed results and data analysis
- Traceability Matrix - Links inputs to outputs to verification tests
- Conclusion - Statement that outputs meet inputs
- Stored in Design History File (DHF)
When verification is required:
- Before design validation
- After design changes
- Before design transfer to manufacturing
- As part of risk mitigation verification
Regulatory requirements:
- FDA 21 CFR 820.30(f) - Design Verification
- ISO 13485:2016 Section 7.3.5 - Design and Development Verification
- EU MDR Technical Documentation requirements
Key principle: Verification uses objective, measurable testing to prove that engineering specifications were met. If verification fails, the design must be modified before proceeding to validation.
Related Terms
More Compliance & Standards
View allLa Regulación del Sistema de Calidad de la FDA que establece los requisitos de Buenas Prácticas de Fabricación actuales (cGMP) para fabricantes de dispositivos médicos en Estados Unidos.
Un examen sistemático e independiente de un Sistema de Gestión de Calidad para determinar si las actividades y resultados de calidad cumplen con los acuerdos planificados y si estos acuerdos se implementan de manera efectiva.
Un enfoque sistemático para investigar, corregir y prevenir problemas de calidad en la fabricación y operaciones de dispositivos médicos.
Un marcado de conformidad obligatorio para dispositivos médicos vendidos en el Espacio Económico Europeo, que indica el cumplimiento de los requisitos de salud, seguridad y medio ambiente de la UE.
Need Help with Global Registration?
Pure Global provides regulatory consulting and AI-powered tools to help medical device companies navigate Global market access.

