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AECL CE-1001-STD
REV.2 |
Standard for Software Engineering of Safety Critical Software |
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| BS-7738-1 |
Specification for Information Systems Products Using SSADM--(Structured Systems Analysis and Design Method) |
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FDA Guidance
Document 3 |
Guidance for the Content of Pre-market Submissions for Software Contained in Medical Devices. (Checklist Available) |
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FDA Guidance
Document 4 |
General Principles of Software Validation - Final Guidance for Industry and FDA Staff (Checklist Available) |
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| IEC 60601-1-4 |
Medical Electrical Equipment--Part 1: General Requirements for Safety-4. Collateral Standard: Programmable Electrical Medical Systems (Checklist Available) |
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| IEC 62304 |
Medical device software - Software life cycle processes (Checklist Available) |
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| IEEE 1012 |
Software Verification and Validation |
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| IEEE 1074 |
Standard for Developing a Software Project Life Cycle Process |
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| IEEE 1220 |
Standard for Application and Management of the Systems Engineering Process |
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| IEEE 16085 |
Software Life Cycle Processes - Risk Management |
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| ISO 17894 |
Ships and marine technology - Computer applications - General principles for the development and use of programmable electronic systems in marine applications |
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| ISO/IEC 12207:2008 |
Systems and software engineering-Software life cycle processes (Checklist Available) |
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| ISO/IEC 14102 |
Guideline for the Evaluation and Selection of CASE Tools |
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| ISO/IEC 14764 |
Software Engineering - Software Life Cycle Processes - Maintenance |
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| ISO/IEC 15288:2008 |
Systems and software engineering-System life cycle processes(Checklist Available) (Discounted Combo Set of 12207 and 15288 Standards (save 5%) |
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| ISO/IEC 15504-2 |
Software Process Assessment- Part 2: A Reference Model for Processes and Process Capability |
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| ISO/IEC TR 24748-1 |
Systems and software engineering - Life cycle management - Part 1: Guide for life cycle management |
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