SaMD (Software as a Medical Device) is 하드웨어 의료기기의 일부가 아니면서 하나 이상의 의료 목적을 수행하는 독립형 소프트웨어.
Complete Guide to SaMD
Software as a Medical Device (SaMD) is defined by the International Medical Device Regulators Forum (IMDRF) as software intended to be used for one or more medical purposes that perform these purposes without being part of a hardware medical device.
Key characteristics of SaMD:
- Standalone software with medical purpose
- Not required to be part of hardware device
- Can run on general computing platforms
- May be marketed independently of hardware
- Subject to medical device regulations
IMDRF SaMD classification framework:
The IMDRF categorizes SaMD based on two dimensions:
- Healthcare situation/condition (Critical, Serious, Non-Serious)
- Significance of information (Treat/Diagnose, Drive Clinical Management, Inform Clinical Management)
This creates four risk categories:
- Category I - Low risk (e.g., wellness apps)
- Category II - Moderate risk (e.g., clinical decision support)
- Category III - Moderate-high risk (e.g., diagnostic imaging analysis)
- Category IV - High risk (e.g., software for critical treatment decisions)
IEC 62304 software lifecycle requirements:
SaMD must comply with IEC 62304, which defines software development lifecycle processes:
- Software development planning
- Requirements analysis and specification
- Architectural and detailed design
- Unit implementation and verification
- Integration and testing
- Release and maintenance
- Risk management throughout lifecycle
Common SaMD examples:
- Mobile diagnostic applications
- Clinical decision support systems
- Medical imaging analysis software
- Patient monitoring algorithms
- Radiation therapy planning systems
- Laboratory information systems with clinical functionality
Regulatory pathways:
- USA (FDA) - 510(k), De Novo, or PMA depending on risk
- EU (MDR) - Class I, IIa, IIb, or III classification
- Canada - Class I-IV classification
- Japan (PMDA) - Class I-IV classification
Cybersecurity and data privacy: SaMD requires special attention to cybersecurity, data protection (GDPR, HIPAA), and regular software updates for security vulnerabilities.
Related Terms
More Compliance & Standards
View all미국 의료기기 제조업체에 대한 현행 우수 제조 관리 기준(cGMP) 요구사항을 규정하는 FDA의 품질 시스템 규정(QSR).
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.
유럽경제지역에서 판매되는 의료기기에 필수인 적합성 표시로, EU 보건, 안전 및 환경 요건 준수를 나타냄.
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