Iec 62304 Checklist Xls May 2026

| ID | Clause | Activity / Checklist Item | Guidance Notes | Actionable Output | | :--- | :--- | :--- | :--- | :--- | | | | | | | | D1 | 5.1.1 | Are input requirements defined? | Capture functional, interface, and performance requirements. | SRS Document | | D2 | 5.1.2 | Are requirements traceable? | Each requirement needs a unique ID. | Traceability Matrix | | D3 | 5.1.3 | Is the content of the SRS complete? | Must include functional, safety, security, and user interface requirements. | Approved SRS | | Design | | | | | | D4 | 5.2 | Has the software architecture been documented? | Define system components, interfaces, and data flows. | Architecture Diagrams | | D5 | 5.3.1 | Has the software detailed design been developed? (Class B/C) | Refine architecture to the unit level. | Detailed Design Docs | | D6 | 5.3.4 | Is there a correspondence between requirements and design? | Verify that every requirement is covered by the design. | Traceability Matrix | | Implementation | | | | | | D7 | 5.4 | Is source code implemented according to design? | Developers must follow coding standards defined in Q2. | Source Code Repo | | D8 | 5.4.2 | Are contributions to the architecture/design recorded? | If coding reveals a design flaw, update the design docs. | Change Request | | Testing | | | | | | D9 | 5.5 | Are Unit Tests defined and executed? (Class B/C) | Test each software unit (function/class) in isolation. | Unit Test Reports | | D10 | 5.6 | Is Integration Testing performed? | Verify interfaces between units/modules. | Integration Test Report | | D11 | 5.7 | Is System Testing performed? | Test against the SRS requirements in the target environment. | System Test Report | | D12 | 5.7.4 | Are regression tests performed after changes? | Ensure changes did not break existing functionality. | Regression Test Report |

This document serves as a comprehensive checklist and implementation guide for IEC 62304:2006+A1:2015 (Medical device software — Software life cycle processes). It is designed to assist software developers, quality managers, and regulatory affairs professionals in establishing compliance for medical device software (SaMD). The content is structured to be easily transferable into an Excel (.xls) format, providing a framework for Software Life Cycle Process management, Safety Classification, and Deliverable Traceability. Iec 62304 Checklist Xls