ISO 9001 Quality Assurance

Model # ISO9001/15

What Is ISO 9001 QA?

A comprehensive Quality Management System that meets the requirements of the International Standard for ISO 9001; 2015. Suitable for Certification by certifying auditors. Meets QMS requirements of National and International prequalification schemes required for tendering and contracts.

Do I need to be certified?

Most tenders allow for an organization to provide evidence of ISO 9001 without certification.

Why become certified with ISO 9001 QA?

A certified ISO 9001 system ensures your company or organization is reaching the highest of quality assurance elements required by the international standards in order to perform national and international projects.

How do I become certified with ISO 9001 QA?

This is a 3 stage process. First, you need to purchase a system that meets the requirements of ISO 9001 and then have it implemented within your company or organization for a period of time showing its working effectiveness. This period also allows you the opportunity to secondly engage in training your employee’s to fulfil their roles and responsibilities within the ISO 9001 framework. There are a number of accredited authorities that can offer one and two-day courses to assist with implementing ISO 9001 within your company. Thirdly once implemented within the ISO 9001 guidelines you are then able to apply for certification by an accredited authority.

Where do I Start?

Assured Health and Safety are committed to helping your business meet the ISO requirements by providing documentation enabling you to take the first step in implement a quality assurance system with a view to certification.

Company Package (0-20 Employees)

Prices shown exclude GST.

ISO 9001/2015 Quality Assurance Components

TABLE OF CONTENTS

• SCOPE
• NORMATIVE REFERENCES
• TERMS AND DEFINITIONS
• CONTEXT OF THE ORGANIZATION
• UNDERSTANDING THE ORGANIZATION AND ITS CONTEXT
• UNDERSTANDING THE NEEDS AND EXPECTATIONS OF INTERESTED PARTIES
• DETERMINING THE SCOPE OF THE QUALITY MANAGEMENT SYSTEM
• LEADERSHIP
• LEADERSHIP AND COMMITMENT
• POLICY
• ORGANIZATION ROLES, RESPONSIBILITIES AND AUTHORITIES
• PLANNING
• ACTIONS TO ADDRESS RISKS AND OPPORTUNITIES
• QUALITY OBJECTIVES AND PLANNING TO ACHIEVE THEM
• PLANNING OF CHANGES
• SUPPORT
• RESOURCES
• COMPETENCE
• AWARENESS
• COMMUNICATION
• DOCUMENTED INFORMATION
• OPERATION
• OPERATIONAL PLANNING AND CONTROL
• REQUIREMENTS FOR PRODUCTS AND SERVICES
• DESIGN AND DEVELOPMENT OF PRODUCTS AND SERVICES
• CONTROL OF EXTERNALLY PROVIDED PROCESSES, PRODUCTS AND SERVICES
• PRODUCTION AND SERVICES PROVISION
• RELEASE OF PRODUCTS AND SERVICES
• CONTROL OF NONCONFORMING OUTPUTS
• PERFORMANCE EVALUATION
• MONITORING, MEASUREMENT, ANALYSIS AND EVALUATION
• INTERNAL AUDIT
• MANAGEMENT REVIEW
• IMPROVEMENT
• GENERAL
• NONCONFORMITY AND CORRECTIVE ACTION
• CONTINUAL IMPROVEMENT

RESOURCE DOCUMENTS

• QUALITY MANAGEMENT PLAN
• INSPECTION TEST PLAN
• ITP CHECKLISTS
• QMS Master List of Controlled Documents
• Drawing, Standards & Specification Register
• Contract Review Form
• Preferred Supplier Recommendation
• Approved Supplier List
• Test Equipment Register
• Test Equipment Report
• External Provider QMS Audit Checklist
• Non-conformance Corrective Action Report
• Non-conformance Corrective Action Register
• Monthly QMS Report
• Customer Complaint Action Form
• Document Change Request
• QMS Audit Schedule
• QA Management Audit Checklist
• Design Plans
• Design Review
• Design Change Request

This item is available for instant download upon purchase!

When ISO 9001 is purchased within the Integrated Management System, you will receive a discount.