Mission-critical and safety-critical systems handbook : design and development for embedded applications

This handbook provides a consolidated, comprehensive information resource for engineers working with mission and safety critical systems. Principles, regulations, and processes common to all critical design projects are introduced in the opening chapters. Expert contributors then offer development m...

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Bibliographic Details
Other Authors: Fowler, Kim R., 1956-
Format: eBook
Language: English
Published: Amsterdam ; Boston : Elsevier/Newnes, ©2010.
Subjects:
Reliability (Engineering)
Fault tolerance (Engineering)
Embedded computer systems > Design and construction.
Safety factor in engineering.
elektronické knihy
electronic books
ISBN: 9780080942551
0080942555
9780750685672
0750685670
1282618520
9781282618527
9786612618529
6612618523
Physical Description: 1 online resource (xiv, 578 pages) : illustrations

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Table of contents

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020 |a 9780750685672 
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020 |a 9781282618527 
020 |a 9786612618529 
020 |a 6612618523 
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245 0 0 |a Mission-critical and safety-critical systems handbook :  |b design and development for embedded applications /  |c edited by Kim Fowler ; technical consultant, Sharfus Draid, Inc. 
260 |a Amsterdam ;  |a Boston :  |b Elsevier/Newnes,  |c ©2010. 
300 |a 1 online resource (xiv, 578 pages) :  |b illustrations 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
504 |a Includes bibliographical references and index. 
506 |a Plný text je dostupný pouze z IP adres počítačů Univerzity Tomáše Bati ve Zlíně nebo vzdáleným přístupem pro zaměstnance a studenty 
520 |a This handbook provides a consolidated, comprehensive information resource for engineers working with mission and safety critical systems. Principles, regulations, and processes common to all critical design projects are introduced in the opening chapters. Expert contributors then offer development models, process templates, and documentation guidelines from their own core critical applications fields: medical, aerospace, and military Readers will gain in-depth knowledge of how to avoid common pitfalls and meet even the strictest certification standards. Particular emphasis is placed on best practices, design tradeoffs, and testing procedures. *Comprehensive coverage of all key concerns for designers of critical systems including standards compliance, verification and validation, and design tradeoffs *Real-world case studies contained within these pages provide insight from experience. 
505 0 |a About the Editor; ; About the Contributors; ; Chapter 1 Best Practices in Mission-Assured, Mission-Critical, and Safety-Critical Systems; ; 1 Roadmap to This Book; ; 1.1 Systems Engineering; ; 1.2 Important Issues; ; 1.3 Material Covered; ; 2 Best Practices; ; 2.1 What and Why?; ; 2.2 Rationale; ; 2.3 Standards and Guidelines for a QMS; ; 3 Project Management and Systems Engineering; ; 3.1 Project Management; ; 3.2 Systems Engineering; ; 3.3 Mission Assurance; ; 4 Process Flows for Developing Products; ; 4.1 Plan, Execute, Review, Report, and Update (PERRU); ; 4.2 Development Processes; ; 4.3 Processes vs. 
505 0 |a Procedures; ; 4.4 General Process Models; ; 4.5 An Example of Phases, Processes, and Procedures; ; 5 Standards; ; 5.1 General Standards Organizations; ; 5.2 Industry-Based Standards Organizations; ; 5.3 Military Standards Organizations; ; 5.4 Aviation and Aerospace Standards Organizations; ; 6 Potential Procedures, Checklists, and Documents; ; 7 Review of Procedures and Processes; ; 7.1 Difference between Procedures and Processes; ; 7.2 Why Review Procedures and Processes?; ; 7.3 Types of Review; ; 7.4 Frequency of Review; ; 7.5 Review Content; ; 7.6 Course of Action, Changes, 
505 0 |a And Updates Following Review; ; 7.7 Review Responsibilities; ; 8 Configuration Management; ; 8.1 Rationale for Configuration Management; ; 8.2 Configuration Management Coverage; ; 8.3 Records Responsibility; ; 8.4 System and Location; ; 8.5 Version Control; ; 8.6 Design Repository; ; 8.7 File Structure; ; 8.8 Obsolete Documents; ; 8.9 Training for Use of the System; ; 9 Documentation; ; 9.1 Rationale for Documentation; ; 9.2 Coverage and Responsibility for Documentation; ; 9.3 Types of Documentation; ; 9.4 Best Practices for Documentation; ; Appendix A: Example Document Outlines; ; Work Order (WO); ; Minutes; ; Problem Report/Corrective Action (PRCA); ; Engineering Change Request (ECR); ; Engineering 
505 0 |a Change Notice (ECN); ; Project Management Plan (PMP); ; Interface Control Documents (ICDs); ; Development Plans; ; Requirements; ; Risk Management Plan; ; Configuration Management Plan; ; Documentation Plan; ; Analysis Reports; ; Design Description; ; Test Plan; ; Operation Plan; ; Metrology Concerns and Procedures; ; Appendix B: Program Management Documents for Project Development; ; Appendix C: Technical Project Documents for Project Development; ; Chapter 2 Failsafe Software Design: Embedded Programming in a Fail-Certain World; ; 1 Software Matters; ; 2 The Essence of Process; ; 3 Three Principles for Design and Coding; ; 3.1 What Does It Mean to Be Failsafe?; ; 3.2 Safety (and Mission) First; ; 3.3 Verification and Redundancy in the Implementation Process; ; 4 
505 0 |a The User Interface; ; 5 Rolling Your Own; ; 6 Hardware as Software: A Thought Exercise in Crossover Thinking; ; 7 Conclusions; ; Chapter 3 Compliance Concerns for Medical Equipment; ; 1 Introduction; ; 2 National and International Requirements; ; 2.1 U.S. 
505 0 |a Requirements; ; 2.2 European Requirements; ; 2.3 Other Countries; ; 3 Medical Device Certification; ; 4 Philosophy of the Standards; ; 5 Evaluation Process; ; 5.1 Preliminary Evaluation; ; 5.2 Testing; ; 5.3 Compliance Reports; ; 5.4 Common Noncompliances; ; 6 Conclusion; ; Chapter 4 Software for Medical Systems; ; 1 Introduction; ; 1.1 Verification and Validation; ; 1.2 Life Cycle Model; ; 2 The Medical Regulatory Environment; ; 2.1 Worldwide Quality System Requirements; ; 2.2 Subpart A: General Provisions; ; 2.3 Subpart B: Quality System Requirements; ; 2.4 Subpart C-Design Controls; ; 2.5 Subpart D-Document Controls; ; 2.6 Subpart E-Purchasing Controls; ; 2.7 Subpart F-Identification 
505 0 |a And Traceability; ; 2.8 Subpart G-Production and Process Controls; ; 2.9 Subpart H-Acceptance Activities, and Subpart I-Nonconforming Product; ; 2.10 Subpart J-Corrective and Preventive Action; ; 2.11 Subpart K-Labeling and Packaging Control; ; 2.12 Subpart L-Handling, Storage, Distribution, 
505 0 |a And Installation; ; 2.13 Subpart M-Records; ; 2.14 Subpart N-Servicing and Subpart O Statistical Techniques; ; 2.15 Post-Market Activities; ; 3 Design Control Explained; ; 3.1 Purpose of Design Control; ; 3.2 Project Planning; ; 3.3 Design Input; ; 3.4 Design Output; ; 3.5 Design Review; ; 3.6 Design Verification and Validation; ; 3.7 Design Changes; ; 3.8 Design History File; ; 3.9 Change Control; ; 3.10 Software Change Control in the Medical Environment; ; 3.11 Software Configuration Management Methods; ; 3.12 Software Problem Resolution; ; 3.13 Problem Evaluation; ; 3.14 Outcomes of the Evaluation Phase; ; 3.15 Corrective Action Process; ; 3.16 Outcomes of the System Test Phase 
505 0 |a ; ; 3.17 Reports; ; 3.18 Software Observation Reporting and Version Control; ; 4 Risk Management; ; 5 Software Verification and Validation in the Context of Design Control; ; 5.1 Software Verification Methods; ; 5.2 Software System Testing; ; 5.3 System Validation (Acceptance Tests); ; 5.4 Traceability; ; 5.5 Metrics; ; 5.6 FDA Regulatory Approval Process; ; 5.7 Device Risk Classes; ; 5.8 Software Level of Concern; ; 5.9 Software Documentation Requirements for Premarket Submissions; ; 5.10 The Review Process and What to Expect from the FDA; ; 6 Special Topics; ; 6.1 Software of Unknown Provenance; ; 6.2 Security and Privacy-HIPAA; ; 7 Summary; ; 8 FAQS; ; Chapter 5 Best Practices in Spacecraft Development 
505 0 |a ; ; 1 Regulations and Standard Practices; ; 1.1 Government Regulations; ; 1.2 Industry Standards; ; 1.3 Commercial Off-the-Shelf; ; 2 Company Processes; ; 2.1 Project Management; ; 2.2 Systems Engineering; ; 2.3 Fault Protection; ; 2.4 Mission Assurance and Safety; ; 2.5 Integration and Test; ; 2.6 Mission Operations; ; 3 Documentation; ; 3.1 Project Documentation; ; 3.2 Corporate Documentation; ; 3.3 Documentation Tools; ; 4 Case Study-New Ho 
590 |a Knovel  |b Knovel (All titles) 
650 0 |a Reliability (Engineering) 
650 0 |a Fault tolerance (Engineering) 
650 0 |a Embedded computer systems  |x Design and construction. 
650 0 |a Safety factor in engineering. 
655 7 |a elektronické knihy  |7 fd186907  |2 czenas 
655 9 |a electronic books  |2 eczenas 
700 1 |a Fowler, Kim R.,  |d 1956-  |1 https://id.oclc.org/worldcat/entity/E39PCjFQHMcGYcWXVBbVd4x343 
776 0 8 |i Print version:  |t Mission-critical and safety-critical systems handbook.  |d Amsterdam ; Boston : Elsevier/Newnes, ©2010  |z 9780750685672  |w (DLC) 2009038373  |w (OCoLC)454361096 
856 4 0 |u https://proxy.k.utb.cz/login?url=https://app.knovel.com/hotlink/toc/id:kpMCSCSHDI/mission-critical-and?kpromoter=marc  |y Full text 

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