50126-1:5 | Railway RAMS | 0 |
50126-1:5.6.3 | Derivation of railway-specific influencing factors | 0 |
50126-1:5.6.4 | Human factors | 0 |
50126-1:5.7.2 | RAMS specification | 0 |
50126-1:5.8 | Risk based approach | 0 |
50126-1:5.9.2 | Reduction of risks related to safety | 0 |
50126-1:5.9.3 | Reduction of risks related to RAM | 0 |
50126-1:6 | Management of railway RAMS: general requirements | 0 |
50126-1:6.2 | Life cycle for the system under consideration | 0 |
50126-1:6.3 | Risk assessment | 0 |
50126-1:6.4 | Organisational requirements | 0 |
50126-1:6.4.2 | Organisational requirements | 0 |
50126-1:6.5 | Application of this standard and adaptability to project scope and size | 0 |
50126-1:6.5.1 | General requirements and tailoring | 0 |
50126-1:6.5.2 | Complex systems with different hierarchical levels | 0 |
50126-1:6.5.3 | Renewal within existing systems | 0 |
50126-1:6.5.4 | Re-use or adaptation of a system with previous acceptance | 0 |
50126-1:6.6 | General requirements on RAMS documentation | 0 |
50126-1:6.7 | Verification and validation | 0 |
50126-1:6.7.2 | Verification | 0 |
50126-1:6.7.3 | Validation | 0 |
50126-1:6.8 | Independent safety assessment | 0 |
50126-1:6.8.2 | Independent safety assessment activities | 0 |
50126-1:7 | RAMS life cycle | 0 |
50126-1:7.1 | Life cycle general requirements and modification impact analysis | 0 |
50126-1:7.10 | Phase 9: System validation | 0 |
50126-1:7.11 | Phase 10: System acceptance | 0 |
50126-1:7.12 | Phase 11: Operation, maintenance and performance monitoring | 0 |
50126-1:7.13 | Phase 12: Decommissioning | 0 |
50126-1:7.2 | Phase 1: Concept | 0 |
50126-1:7.3 | Phase 2: System definition and operational context | 0 |
50126-1:7.3.2.2 | RAM plan | 0 |
50126-1:7.3.2.3 | Safety plan | 0 |
50126-1:7.4 | Phase 3: Risk analysis and evaluation | 0 |
50126-1:7.4.2.2 | Hazard log | 0 |
50126-1:7.5 | Phase 4: Specification of system requirements | 0 |
50126-1:7.5.4 | Phase 4 specific validation tasks | 0 |
50126-1:7.6 | Phase 5: Architecture and apportionment of system requirements | 0 |
50126-1:7.7 | Phase 6: Design and implementation | 0 |
50126-1:7.7.4 | Phase 6 specific verification tasks | 0 |
50126-1:7.8 | Phase 7: Manufacture | 0 |
50126-1:7.9 | Phase 8: Integration | 0 |
50126-1:7.9.4 | Phase 8 specific verification tasks | 0 |
50126-1:8.1 | Purpose of a safety case | 0 |
50126-1:8.2 | Content of a safety case | 0 |
50126-1:A | Annex A (informative): RAMS plan | 0 |
50126-1:B | Annex B (informative): RAMS parameters | 0 |
50126-1:C | Annex C (informative): risk matrix examples | 0 |
50126-1:D | Annex D (informative): system definition guidance | 0 |
50126-2:10.1 | Deriving and apportioning system safety requirements | 0 |
50126-2:10.2.1 | Deriving functional safety requirements for electronic systems | 0 |
50126-2:10.2.10 | Demonstration of quantified targets | 0 |
50126-2:10.2.11 | Requirements for basic integrity | 0 |
50126-2:10.2.12 | Prevention of misuse of SILs | 0 |
50126-2:10.2.2 | Apportioning safety requirements | 0 |
50126-2:10.2.3 | Safety integrity factors | 0 |
50126-2:10.2.4 | Functional safety integrity and random failures | 0 |
50126-2:10.2.5 | Systematic aspect of functional safety integrity | 0 |
50126-2:10.2.6 | Balanced requirements controlling random and systematic failures | 0 |
50126-2:10.2.7 | The SIL table | 0 |
50126-2:10.2.8 | SIL allocation | 0 |
50126-2:10.2.9 | Apportionment of TFFR after SIL allocation | 0 |
50126-2:10.3 | Safety integrity for non-electronic systems: application of codes of practice | 0 |
50126-2:11.2 | Causal analysis | 0 |
50126-2:11.3 | Hazard identification (refinement) | 0 |
50126-2:11.4 | Common cause analysis | 0 |
50126-2:5.1 | Risk assessment and hazard control | 0 |
50126-2:5.2.2 | Conducting risk assessment | 0 |
50126-2:5.3 | Outcome of the risk assessment | 0 |
50126-2:5.4 | Hazard control | 0 |
50126-2:5.5 | Revision of risk assessment | 0 |
50126-2:5.6 | Responsibilities | 0 |
50126-2:6.2 | Safety demonstration and safety acceptance process | 0 |
50126-2:6.3 | Responsibility in managing the safety case | 0 |
50126-2:6.4 | Modifications after safety acceptance | 0 |
50126-2:6.5 | Dependencies between safety cases | 0 |
50126-2:6.6 | Relationship between safety cases and system architecture | 0 |
50126-2:7.2 | Early phases of the life cycle (phases 1 to 4): independence of roles | 0 |
50126-2:7.3 | Later phases of the life cycle (from phase 5): independence of roles | 0 |
50126-2:7.4 | Personnel competence | 0 |
50126-2:8.2.2 | The risk model | 0 |
50126-2:8.2.3 | Techniques for the consequence analysis | 0 |
50126-2:8.2.4 | Expert judgement | 0 |
50126-2:8.3.1 | Use of code of practice | 0 |
50126-2:8.3.2 | Use of a reference system | 0 |
50126-2:8.3.3 | Use of explicit risk estimation | 0 |
50126-2:8.4.1 | Quantitative approach | 0 |
50126-2:8.4.2 | Variability using quantitative risk estimates | 0 |
50126-2:8.4.3 | Qualitative and semi-quantitative approaches | 0 |
50126-2:9.3.2 | Functional safety requirements | 0 |
50126-2:9.3.3 | Technical safety requirements | 0 |
50126-2:9.3.4 | Contextual safety requirements | 0 |
50128:0 | Introduction and status: EN 50128:2011 superseded by EN 50716:2023 | 0 |
50128:3 | Terms, definitions and abbreviations | 0 |
50128:4 | Objectives, conformance and software safety integrity levels | 0 |
50128:5 | Software management and organisation | 0 |
50128:5.1 | Organisation, roles and responsibilities | 0 |
50128:5.2 | Personnel competence | 0 |
50128:5.3 | Lifecycle issues and documentation | 0 |
50128:6 | Software assurance | 0 |
50128:6.1 | Software testing | 0 |
50128:6.2 | Software verification | 0 |
50128:6.3 | Software validation | 0 |
50128:6.4 | Software assessment | 0 |
50128:6.5 | Software quality assurance | 0 |
50128:6.6 | Modification and change control | 0 |
50128:6.7 | Support tools and languages | 0 |
50128:7 | Generic software development | 0 |
50128:7.1 | Lifecycle and documentation for generic software | 0 |
50128:7.2 | Software requirements | 0 |
50128:7.3 | Architecture and design | 0 |
50128:7.4 | Component design | 0 |
50128:7.5 | Component implementation and testing | 0 |
50128:7.6 | Integration | 0 |
50128:7.7 | Overall software testing / final validation | 0 |
50128:8 | Development of application data or algorithms: systems configured by application data or algorithms | 0 |
50128:8.4.1 | Application data or algorithms development process | 0 |
50128:8.4.2 | Application requirements specification | 0 |
50128:8.4.3 | Application architecture and design | 0 |
50128:8.4.4 | Application data or algorithms production | 0 |
50128:8.4.5 | Application data or algorithms integration and testing / acceptance | 0 |
50128:8.4.6 | Application data or algorithms validation and assessment | 0 |
50128:8.4.7 | Application data or algorithms preparation procedures and tools | 0 |
50128:8.4.8 | Development of generic software | 0 |
50128:9 | Software deployment and maintenance | 0 |
50128:9.1 | Software deployment | 0 |
50128:9.2 | Software maintenance | 0 |
50128:A | Annex A (normative): criteria for the selection of techniques and measures | 0 |
50128:A.1 | Table A.1: lifecycle issues and documentation (5.3) | 0 |
50128:A.10 | Table A.10: software maintenance (9.2) | 0 |
50128:A.11 | Table A.11: data preparation techniques (8.4) | 0 |
50128:A.12-A.23 | Annex A.2 (normative): detailed tables A.12 to A.23 | 0 |
50128:A.2 | Table A.2: software requirements specification (7.2) | 0 |
50128:A.3 | Table A.3: software architecture (7.3) | 0 |
50128:A.4 | Table A.4: software design and implementation (7.3, 7.4 and 7.5) | 0 |
50128:A.5 | Table A.5: verification and testing (6.2 and 7.4) | 0 |
50128:A.6 | Table A.6: integration (7.3 and 7.6) | 0 |
50128:A.7 | Table A.7: overall software testing (6.2 and 7.2) | 0 |
50128:A.8 | Table A.8: software analysis techniques (6.3) | 0 |
50128:A.9 | Table A.9: software quality assurance (6.5) | 0 |
50128:B | Annex B (normative): key software roles and responsibilities | 0 |
50128:C | Annex C (informative): documents control summary | 0 |
50128:D | Annex D (informative): bibliography of techniques | 0 |
50129:0 | Introduction and status: EN 50129:2018, its corrigendum and the 2025 revision | 0 |
50129:3 | Terms, definitions and abbreviations | 0 |
50129:4 | Overall framework of this document | 0 |
50129:5 | Requirements for developing safety-related electronic systems | 0 |
50129:5.1 | Introduction: the conditions for safety acceptance | 0 |
50129:5.2 | The quality management process | 0 |
50129:5.3 | The safety management process | 0 |
50129:5.3.10 | Safety verification | 0 |
50129:5.3.11 | Safety validation | 0 |
50129:5.3.12 | Safety qualification tests | 0 |
50129:5.3.13 | Safety-related application conditions | 0 |
50129:5.3.14 | Safety justification | 0 |
50129:5.3.15 | Independent safety assessment | 0 |
50129:5.3.2 | Guideline for structuring documentation | 0 |
50129:5.3.3 | Safety life cycle | 0 |
50129:5.3.4 | Safety organization | 0 |
50129:5.3.5 | Safety plan | 0 |
50129:5.3.6 | Hazard log | 0 |
50129:5.3.7 | Safety requirements specification | 0 |
50129:5.3.8 | System design for safety | 0 |
50129:5.3.9 | Safety operation and maintenance plan | 0 |
50129:6 | Requirements for elements following different life cycles | 0 |
50129:6.2 | Use of pre-existing items | 0 |
50129:6.3 | Safety-related tools for electronic systems | 0 |
50129:6.4 | Physical security and IT-security | 0 |
50129:7 | The Safety Case: structure and content | 0 |
50129:7.1 | The Safety Case structure | 0 |
50129:7.2 | The Technical Safety Report | 0 |
50129:7.3 | Generic and Specific Safety Cases | 0 |
50129:7.4 | Provisions for the Specific Application Safety Case | 0 |
50129:7.5 | Dependencies between Safety Cases | 0 |
50129:8 | System safety acceptance and subsequent phases | 0 |
50129:8.1 | System safety acceptance process | 0 |
50129:8.2 | Operation, maintenance and performance monitoring | 0 |
50129:8.3 | Modification and retrofit | 0 |
50129:8.4 | Decommissioning and disposal | 0 |
50129:A | Annex A (normative): safety integrity levels | 0 |
50129:A.2 | Safety requirements | 0 |
50129:A.3 | Safety integrity | 0 |
50129:A.4 | Determination of safety integrity requirements | 0 |
50129:A.4.2 | Risk assessment | 0 |
50129:A.4.3 | Hazard control | 0 |
50129:A.4.4 | Identification and treatment of new hazards arising from design | 0 |
50129:A.5 | Allocation of SILs | 0 |
50129:A.5.1 | General aspects | 0 |
50129:A.5.2 | Relationship between SIL and associated TFFR | 0 |
50129:B | Annex B (normative): management of faults for safety-related functions | 0 |
50129:B.2 | General concepts | 0 |
50129:B.2.1 | Detection and negation times | 0 |
50129:B.2.2 | Composition of two independent items | 0 |
50129:B.3 | Effects of faults | 0 |
50129:B.3.1 | Effects of single faults | 0 |
50129:B.3.2 | Influences between items | 0 |
50129:B.3.3 | Detection of single faults | 0 |
50129:B.3.4 | Action following detection (retention of safe state) | 0 |
50129:B.3.5 | Effects of multiple faults | 0 |
50129:B.3.6 | Defence against systematic faults | 0 |
50129:C | Annex C (normative): identification of hardware component failure modes | 0 |
50129:C.2 | General procedure | 0 |
50129:C.3 | Procedure for integrated circuits | 0 |
50129:C.4 | Procedure for components with inherent physical properties | 0 |
50129:C.5 | General provisions concerning component failure modes | 0 |
50129:D | Annex D (informative): example of THR/TFFR/FR apportionment and SIL allocation | 0 |
50129:E | Annex E (normative): techniques and measures for the avoidance of systematic faults and the control of random and systematic faults | 0 |
50129:F | Annex F (informative): guidance on user programmable integrated circuits | 0 |
50129:G | Annex G (informative): changes compared to EN 50129:2003 | 0 |
50129:ZZ | Annex ZZ (informative): relationship with the essential requirements of Directive 2008/57/EC | 0 |