INTRODUCTIONInstitutions Promoting Quality Movement in IndiaBureau of Indian Standards (BIS)Quality Council of IndiaCII Institute of QualityDevelopment of the ISO 9000 StandardsISO 9001:2015Benefits of ISO 9001 CertificationQuality Management PrinciplesQuality Management Systems (QMS): An IntroductionProcess ApproachISO 9001:2015 Quality Management Systems RequirementsBasic ClausesISO 9000:2015, Quality Management Systems – Fundamentals and VocabularyISO 9001:2015 StructureMain ClausesClause 4.1: Understanding the Organisation and its ContextClause 4.2: Understanding the Needs and Expectations of Interested PartiesClause 4.3: Determining the Scope of the Quality Management SystemClause 4.4: Quality Management System and its ProcessesClause 5: LeadershipClause 5.1: Leadership and CommitmentClause 5.2: Quality PolicyClause 5.3: Organisational Roles, Responsibilities, and AuthoritiesClause 6: PlanningClause 6.1: Actions to Address Risks and OpportunitiesClause 6.2: Quality Objectives and Planning to Achieve themClause 6.3: Planning of ChangesClause 7: SupportClause 7.1: ResourcesClause 7.2: CompetenceClause 7.3: AwarenessClause 7.4: CommunicationClause 7.5: Documented InformationClause 8: OperationClause 8.1: Operational Planning and ControlClause 8.2: Determination of Requirements for Products and ServicesClause 8.3: Design and Development of Products and ServicesClause 8.4: Control of Externally Provided Products and ServicesClause 8.5: Production and Service ProvisionClause 8.6: Release of Products and ServicesClause 8.7: Control of Nonconforming Process Outputs, Products, and ServicesClause 9: Performance EvaluationClause 9.1: Monitoring, Measurement, Analysis, and EvaluationClause 9.2: Internal AuditClause 9.3: Management ReviewClause 10: ImprovementClause 10.1: GeneralClause 10.2: Nonconformity and Corrective ActionClause 10.3: Continual ImprovementAnnex A (informative): Clarification of New Structure, Terminology, and ConceptsAnnex B (informative): Other International Standards on Quality Management and QMS Developed by ISO/TC 176Mandatory Documents and Records Required by ISO 9001:2015Non-Mandatory DocumentsISO 14000 SeriesKey Benefits of Environmental Management SystemRequirements of ISO 14001:2015Mandatory Documents and Records Required by ISO 14001:2015Occupational Health and Safety Management System (OH&S MS)ISO 45001:2018Requirements of ISO 45001:2018Mandatory Documents Required by ISO 45001:2018Mandatory Records Required by ISO 45001:2018Non-Mandatory DocumentsIntegrated Management SystemThe Annex SL Management System TemplateAuditing Management SystemsGuidelines for Auditing Management Systems (19011:2018)5 Managing an Audit Programme5.1 General5.2. Establishing audit programme objectives5.3 Determining and Evaluating Audit Programme Risks and Opportunities5.4 Establishing the audit programme5.5 Implementing audit programme5.6 Monitoring Audit Programme5.7 Reviewing and Improving Audit Programme6 Conducting an Audit6.1 General6.2 Initiating Audit6.3 Preparing Audit Activities6.4 Conducting Audit Activities6.5 Preparing and distributing audit report6.6 Completing Audit6.7 Conducting Audit Follow-up7 Competence and Evaluation of Auditors7.1 General7.2 Determining Auditor Competence7.3 Establishing Auditor Evaluation Criteria7.4 Selecting Appropriate Auditor Evaluation Method7.5 Conducting Auditor Evaluation7.6 Maintaining and Improving Auditor CompetenceIntegrated ISO Management System AuditsThird-Party Management SystemsAudit (Certification Audits)ISO/IEC 17021:2015Four Phases of an AuditSteps to ISO CertificationInternational Organisation for Standardisation RegistrarsSummaryKey TermsCase Study: Total Quality Management at Hyundai MotorsShort-Answer QuestionsMatch the FollowingDiscussion QuestionsProjectsReferences