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1.1 Course Introduction

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Quality

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Management System

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Quality Management System(QMS)

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Quality Policy

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Quality objective

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Context

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Documented Information

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Measurement , Monitoring

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Statutory , Regulatory Requirement

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Review, Verification , Validation

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Audit, Non-Conformity, Correction and Corrective Action

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Conformity and Non conformity

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Correction , Corrective Action

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Improvement

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Quiz- Terms and Definition-Management System Common

14 questions

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Workshop-Mix and Match-Terms and Definitions

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Purpose and Benefit

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ISO 9001:2015 Model and 10 Element HLS-Overview

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1. Scope

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2. Normative Reference

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3.Terms and definitions

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4.Context of the organization

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5. Leadership

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6. Planning

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7. Support

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8. Operation

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9. Performance evaluation

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10. Improvement

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Conformity Assessment Case#1

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Conformity Assessment Case#2

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Conformity Assessment Case#3

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Conformity Assessment Case#4

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Conformity Assessment Case#5

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Conformity Assessment Case#6

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Conformity Assessment Case#7

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Conformity Assessment Case#8-Audit Frequency

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Conformity Assessment Case#9-Identify what has gone wrong and Indicate Clause No./s.

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Conformity Assessment Case#10

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First Party Second Party Third Party Audit

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Audit Process flowchart (ISO 19011)

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Audit Method

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Audit Parameters, Scope-objectives and Criteria

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Types of Audit

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2 stage Audit Approach-Stage 1 Audit

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2 stage Audit Approach-Stage 2 Audit

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Certification Audit Process Steps

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Remote Audit

10

Special Audits-Extension/reduction of scope

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Special Audits-Short Notice

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Special Audits- suspension, withdrawal

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Quiz-Conducting Audit

12 questions

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WSE 3 : Adequacy of Documented Information-During Tutor Guided Live Sessions (Case study : Universal Motors)

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WSE 4 : Auditing Top Management (Role Play During Stage 2 Audit)

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Check list

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Advantage and Draw back

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Audit Check list-Top Management Commitment

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Prepare a Check list-Purchasing Process

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Prepare a Check List- Measuring and Monitoring Resource

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Prepare a Check List-requirement for products and services

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Prepare a Check List-Product and Service Provision

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Prepare a Check List-Internal Audit

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Prepare a Check list-Nonconforming Output

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Prepare a Check List-Management Review

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Prepare a Check List-Improvement

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WSE 6 : Opening Meeting Role Play

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WSE 7: Auditing Competence Awareness And Training -UMS Case study

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WSE 8. Control of M

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WSE 9 : -Customer Related Process -External and Internal Communication

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WSE 10: Procurement and outsourcing

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WSE 11: Planning for Product Realization

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WSE 12: Product and Service Provision

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WSE 13: Measurement and monitoring ,NC Output, Release of Products

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WSE 14: Auditing Internal Audit Process

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WSE 15: Prepare a Certification Audit Report

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WSE 16: Close out Meeting Role Play

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WSE 17: Conducting a Follow-up Audit

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Certification and Accreditation

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Accreditation

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Principles of Credible Certification

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IAF , Accreditation and Certification Bodies Hierarchy

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Credible certification process

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Quiz Certification and Accreditation

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Briefly Explain the Importance of Confidentiality in an Audit

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Briefly Explain Risk Based approach to Audit

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Briefly Explain the evidence based approach to Audit

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Register for CQI/IRCA Exam.

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CQI/IRCA Examination Process