Unverified50% confidenceFactExact time
The FDA's IEC 62304 standard has strict requirements for the development lifecycle of medical device software, requiring every line of code to be traceable to requirement specifications.
1
Sources
50%
Confidence
Long-term
Relevance
9/2/2026
First Seen
Sources
Related Entities
Related Claims
Unverified工业程序推理过程的可追溯性符合工业安全领域可解释性要求，在功能安全标准（如IEC 61508）严格的场景下是安全体系的一部分68% similarUnverified国际标准 ISO/IEC 26514 专门规范软件用户文档的设计与开发，涵盖文档结构、可用性测试和准确性要求66% similarUnverifiedEnterprise-grade code requires comprehensive exception handling and fallback strategies, standardized logging and monitoring instrumentation, strict security protection (SQL injection, XSS, access control), observability design, and data consistency guarantees62% similarUnverified安全编码规范要求调用外部程序时应始终使用绝对路径，或严格校验可执行文件的来源与签名59% similar
Cite This Claim
Stable URI
https://kongchang.com/claim/842918API
curl https://kongchang.com/api/v1/knowledge/claims/842918MCP
get_claim(id=842918)