{"product_id":"guidelines-for-revalidating-a-process-hazard-analysis-hardback-9781119643609","title":"Guidelines for Revalidating a Process Hazard Analysis (Hardback) 9781119643609","description":"\u003cfont face=\"Georgia\"\u003e\r\n\u003cp\u003e\u003cfont size=\"6\"\u003eGuidelines for Revalidating a Process Hazard Analysis\u003c\/font\u003e\u003cbr\u003e\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\u003c\/p\u003e\n\u003cp\u003e\u003cfont size=\"3\"\u003e9781119643609, Wiley\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eHardback, published 25 October 2022\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e240 pages\u003cbr\u003e23.4 x 15.8 x 2 cm, 0.386 kg\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\r\n\r\n\r\n\u003cp align=\"justify\"\u003e\u003cstrong\u003e\u003cfont size=\"3\"\u003e\u003cp\u003e\u003cb\u003eGUIDELINES FOR REVALIDATING A PROCESS HAZARD ANALYSIS\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eThis book is derived from the experience of many companies in the chemical and hydrocarbon processing industries, and presents demonstrated, concise, and common sense approaches for a resource-effective revalidation of process hazard analyses (PHAs). It includes flowcharts, checklists, and worksheets that provide invaluable assistance to the revalidation process.\u003c\/p\u003e \u003cp\u003eThe new edition, now as a guideline, provides a compete and thorough update of the first book and will provide much needed and requested guidance on PHA Revalidations including evaluating Prior PHA Studies, Identifying an Appropriate Revalidation Methodology, Preparing and Conducting the Revalidation Study Sessions, and Documenting the Revalidation Study.\u003c\/p\u003e\u003c\/font\u003e\u003c\/strong\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e\u003cp\u003eList of Tables ix\u003c\/p\u003e \u003cp\u003eList of Figures ix\u003c\/p\u003e \u003cp\u003eAcronyms and Abbreviations x\u003c\/p\u003e \u003cp\u003eGlossary and Nomenclature xii\u003c\/p\u003e \u003cp\u003eAcknowledgments xiv\u003c\/p\u003e \u003cp\u003ePreface xvi\u003c\/p\u003e \u003cp\u003eDedication xvii\u003c\/p\u003e \u003cp\u003e\u003cb\u003eIntroduction xix\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eObjective of this Book xix\u003c\/p\u003e \u003cp\u003eScope of this Book xix\u003c\/p\u003e \u003cp\u003eHow to Use This Guidelines Book xx\u003c\/p\u003e \u003cp\u003e\u003cb\u003e1 Overview of the PHA Revalidation Process 1\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1.1 What is a PHA and What is a PHA Intended to Accomplish? 2\u003c\/p\u003e \u003cp\u003e1.2 Overview of Typical PHA Activities 4\u003c\/p\u003e \u003cp\u003e1.2.1 PHA Core Methodology 4\u003c\/p\u003e \u003cp\u003e1.2.2 PHA Complementary Analyses 6\u003c\/p\u003e \u003cp\u003e1.3 General Risk Assessment Principles 8\u003c\/p\u003e \u003cp\u003e1.3.1 Risk and Risk Tolerance 8\u003c\/p\u003e \u003cp\u003e1.3.2 Supplemental Risk Assessments 9\u003c\/p\u003e \u003cp\u003e1.4 PHA Revalidation Objectives 11\u003c\/p\u003e \u003cp\u003e1.5 PHA Revalidation Concept 14\u003c\/p\u003e \u003cp\u003e1.6 PHA Revalidation Cycle 16\u003c\/p\u003e \u003cp\u003e1.7 The Role of a PHA Revalidation Procedure 19\u003c\/p\u003e \u003cp\u003e1.8 Relationship of RBPS Pillars to a PHA Revalidation 21\u003c\/p\u003e \u003cp\u003e\u003cb\u003e2 PHA Revalidation Requirements 23\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e2.1 External Legal\/Regulatory Requirements 23\u003c\/p\u003e \u003cp\u003e2.1.1 General Obligations 25\u003c\/p\u003e \u003cp\u003e2.1.2 Specific RAGAGEPs 26\u003c\/p\u003e \u003cp\u003e2.2 Internal Company Policy Requirements 28\u003c\/p\u003e \u003cp\u003e2.2.1 Compliance-Driven Policies 29\u003c\/p\u003e \u003cp\u003e2.2.2 EHS-Driven Policies 29\u003c\/p\u003e \u003cp\u003e2.2.3 Value-Driven Policies 30\u003c\/p\u003e \u003cp\u003e2.3 Internal Company Drivers That Impact Revalidation 31\u003c\/p\u003e \u003cp\u003e2.4 Principles for Successful Definition of Revalidation Requirements 33\u003c\/p\u003e \u003cp\u003e\u003cb\u003e3 Evaluating the Prior PHA 35\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e3.1 Prior PHA Essential Criteria 38\u003c\/p\u003e \u003cp\u003e3.1.1 Prior PHA Methodology Used 38\u003c\/p\u003e \u003cp\u003e3.1.2 Prior PHA Inputs 40\u003c\/p\u003e \u003cp\u003e3.1.3 Prior PHA Scope 43\u003c\/p\u003e \u003cp\u003e3.1.4 Drawing Essential Criteria Conclusions 46\u003c\/p\u003e \u003cp\u003e3.2 Prior PHA Quality and Completeness 48\u003c\/p\u003e \u003cp\u003e3.2.1 Application of Analysis Method(s) 49\u003c\/p\u003e \u003cp\u003e3.2.2 Level of Detail and Accuracy of the Core Analysis 50\u003c\/p\u003e \u003cp\u003e3.2.3 Logic Errors and Inconsistencies in the Analysis 56\u003c\/p\u003e \u003cp\u003e3.2.4 Failure to Document Hazards 58\u003c\/p\u003e \u003cp\u003e3.2.5 Improper Application of Risk Tolerance 59\u003c\/p\u003e \u003cp\u003e3.2.6 Drawing Quality and Completeness Conclusions 60\u003c\/p\u003e \u003cp\u003e3.3 Prior PHA Topics for Additional Evaluation 61\u003c\/p\u003e \u003cp\u003e3.3.1 Status of Prior PHA Recommendations 61\u003c\/p\u003e \u003cp\u003e3.3.2 Complementary Analyses and Supplemental Risk Assessments 62\u003c\/p\u003e \u003cp\u003e3.3.3 Opportunity to Learn and Capture Information 62\u003c\/p\u003e \u003cp\u003e3.3.4 Continuous Improvement 63\u003c\/p\u003e \u003cp\u003e3.3.5 PHA Documentation Software Changes 63\u003c\/p\u003e \u003cp\u003e3.3.6 Time Since the Previous Redo 63\u003c\/p\u003e \u003cp\u003e3.4 Principles for Successful Prior PHA Evaluation 64\u003c\/p\u003e \u003cp\u003e\u003cb\u003e4 Evaluating Operating Experience Since the Prior PHA 67\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e4.1 Operating Experience Influence on Revalidation 68\u003c\/p\u003e \u003cp\u003e4.2 Types of Operating Experience That Should Be Considered 68\u003c\/p\u003e \u003cp\u003e4.2.1 MOC and PSSR Records 69\u003c\/p\u003e \u003cp\u003e4.2.2 Incident Reports 75\u003c\/p\u003e \u003cp\u003e4.2.3 Routine Maintenance Records 77\u003c\/p\u003e \u003cp\u003e4.2.4 Audit Results 78\u003c\/p\u003e \u003cp\u003e4.2.5 Organizational Changes Not Addressed by MOCs 79\u003c\/p\u003e \u003cp\u003e4.2.6 Metrics and Overall Performance 82\u003c\/p\u003e \u003cp\u003e4.3 How Operating Experience Affects the Revalidation 83\u003c\/p\u003e \u003cp\u003e4.4 Principles for Successful Operating Experience Evaluation 85\u003c\/p\u003e \u003cp\u003e\u003cb\u003e5 Selecting An Appropriate PHA Revalidation Approach 89\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e5.1 Revalidation Approaches 90\u003c\/p\u003e \u003cp\u003e5.1.1 Update 90\u003c\/p\u003e \u003cp\u003e5.1.2 Redo 92\u003c\/p\u003e \u003cp\u003e5.1.3 Combining Update and Redo in a Revalidation 94\u003c\/p\u003e \u003cp\u003e5.2 Selecting the Revalidation Options 97\u003c\/p\u003e \u003cp\u003e5.2.1 Have the Requirements Changed Significantly? 98\u003c\/p\u003e \u003cp\u003e5.2.2 Is the Prior PHA Deficient or Unacceptable? 100\u003c\/p\u003e \u003cp\u003e5.2.3 Are There Too Many Changes or Significant Revelations in Operating Experience? 101\u003c\/p\u003e \u003cp\u003e5.3 Principles for Successful Revalidation Approach Selection 103\u003c\/p\u003e \u003cp\u003e\u003cb\u003e6 Preparing for PHA Revalidation Meetings 105\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e6.1 Planning the Revalidation Meetings 106\u003c\/p\u003e \u003cp\u003e6.1.1 Establishing the Revalidation Scope 106\u003c\/p\u003e \u003cp\u003e6.1.2 Selecting Team Members 108\u003c\/p\u003e \u003cp\u003e6.1.3 Estimating Schedule, Time, and Resources 110\u003c\/p\u003e \u003cp\u003e6.2 Identifying and Collecting Information 113\u003c\/p\u003e \u003cp\u003e6.2.1 Determining Information Requirements 113\u003c\/p\u003e \u003cp\u003e6.2.2 Distributing Information 117\u003c\/p\u003e \u003cp\u003e6.3 Reviewing and Preparing Information 117\u003c\/p\u003e \u003cp\u003e6.3.1 Prior PHA Reports and Related Documentation 117\u003c\/p\u003e \u003cp\u003e6.3.2 Prior PHA Recommendation Resolution Status 118\u003c\/p\u003e \u003cp\u003e6.3.3 MOC and PSSR Records 120\u003c\/p\u003e \u003cp\u003e6.3.4 Audit Results 126\u003c\/p\u003e \u003cp\u003e6.3.5 Incident Reports 126\u003c\/p\u003e \u003cp\u003e6.3.6 Current Piping and Instrument Diagrams 127\u003c\/p\u003e \u003cp\u003e6.3.7 Current Operating Procedures 127\u003c\/p\u003e \u003cp\u003e6.3.8 Special Considerations for Complementary Analyses and Supplemental Risk Assessments 128\u003c\/p\u003e \u003cp\u003e6.4 Principles for Successful Revalidation Preparation 129\u003c\/p\u003e \u003cp\u003e\u003cb\u003e7 Conducting PHA Revalidation Meetings 131\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e7.1 Applying Analysis Methodologies 131\u003c\/p\u003e \u003cp\u003e7.1.1 Revalidation of the Core Analysis 132\u003c\/p\u003e \u003cp\u003e7.1.2 Revalidation of Complementary Analyses 134\u003c\/p\u003e \u003cp\u003e7.1.3 Revalidation of Supplemental Risk Assessments 137\u003c\/p\u003e \u003cp\u003e7.2 Facilitating Effective Revalidation Meetings 139\u003c\/p\u003e \u003cp\u003e7.2.1 Team Composition 139\u003c\/p\u003e \u003cp\u003e7.2.2 Meeting Kickoff 140\u003c\/p\u003e \u003cp\u003e7.2.3 Meeting Productivity 143\u003c\/p\u003e \u003cp\u003e7.3 Revalidation Meeting Conclusion 149\u003c\/p\u003e \u003cp\u003e7.4 Principles for Successful Revalidation Meetings 151\u003c\/p\u003e \u003cp\u003e\u003cb\u003e8 Documenting and Following Up on a PHA Revalidation 155\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e8.1 Documentation Approaches 156\u003c\/p\u003e \u003cp\u003e8.2 Report and Its Contents 160\u003c\/p\u003e \u003cp\u003e8.3 Recommendations and Follow-Up 161\u003c\/p\u003e \u003cp\u003e8.4 Records Retention and Distribution 163\u003c\/p\u003e \u003cp\u003e8.5 Principles for Successful Documentation and Follow-Up 165\u003c\/p\u003e \u003cp\u003eReferences 167\u003c\/p\u003e \u003cp\u003e\u003cb\u003eAppendices 171\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eAppendix A Essential Criteria Checklist 171\u003c\/p\u003e \u003cp\u003eAppendix B PHA Quality and Completeness Checklist 175\u003c\/p\u003e \u003cp\u003eAppendix C Example Change Summary Worksheet 181\u003c\/p\u003e \u003cp\u003eAppendix D Checklist of Process, Facility, and Human Factors Changes 183\u003c\/p\u003e \u003cp\u003eAppendix E Example Facility Siting Checklists 187\u003c\/p\u003e \u003cp\u003eAppendix F Example Human Factors Checklists 199\u003c\/p\u003e \u003cp\u003eAppendix G Example External Events Checklist 209\u003c\/p\u003e \u003cp\u003eIndex 215\u003c\/p\u003e\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eSubject Areas: Industrial chemistry \u0026amp; manufacturing technologies [\u003ca title=\"See our other books on Industrial chemistry \u0026amp; manufacturing technologies\" href=\"https:\/\/freshlyprintedbooks.co.uk\/search?q=%22Industrial%20chemistry%20\u0026amp;%20manufacturing%20technologies%20%5BTD%5D%22\"\u003eTD\u003c\/a\u003e]\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\u003c\/font\u003e","brand":"Wiley-AIChE","offers":[{"title":"Brand New","offer_id":52516604739864,"sku":"9781119643609","price":85.67,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0730\/2037\/5320\/files\/9781119643609.jpg?v=1786691408","url":"https:\/\/freshlyprintedbooks.co.uk\/products\/guidelines-for-revalidating-a-process-hazard-analysis-hardback-9781119643609","provider":"Freshly Printed Books","version":"1.0","type":"link"}