Design Verification is 객관적인 테스트 및 분석을 통해 설계 출력이 설계 입력을 충족함을 확인하는 테스트 및 증거입니다.
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.
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품질 활동 및 결과가 계획된 약정을 준수하는지 여부와 이러한 약정이 효과적으로 구현되고 있는지 확인하기 위한 품질 관리 시스템의 체계적이고 독립적인 검사.
의료기기 제조 및 운영에서 품질 문제를 조사, 시정 및 예방하기 위한 체계적인 접근 방식.
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