ISO 9001 – an overview Tor Stålhane IDI / NTNU. ISO 9001 and software development ISO 9001 is a general standard – equally applicable to software development.

Slides:



Advertisements
Similar presentations
ISO 9001:2000 Documentation Requirements
Advertisements

Transition from Q1- 8th to Q1- 9th edition
Exercise 1 TDT 4235 Tor Stålhane IDI / NTNU. Intro The strength of ISO9001 and many other standards is that they focus on “What shall be done” and leave.
DOCUMENTATION REQUIREMENTS Based on ISO 9001:2008
Welcome to ISO 9000 for Managers
Understanding the Requirements Qimpro Standards Organization
ISO 9001 : 2000.
EPSON STAMPING ISO REV 1 2/10/2000.
The ISO 9002 Quality Assurance Management System
Prepared by Long Island Quality Associates, Inc. ISO 9001:2000 Documentation Requirements Based on ISO/TC 176/SC 2 March 2001.
ISO 9001:2000 Intro Presented By: Brad D. Agenda Overview of QMS Fundamentals ISO 9001:2000 Overview & Requirements.
ASPEC Internal Auditor Training Version
ISO 9000 Certification ISO 9001 and ISO
The application of ISO 9001 to agile software development
ISO 9001:2008: Key changes and transition process
THE PRINCIPLES OF QUALITY MANAGEMENT. DEFINING QUALITY Good Appearance? High Price? The Best? Particular Specification? Not necessarily, but always: Fitness.
4. Quality Management System (QMS)
4. Quality Management System (QMS)
Fundamentals of ISO.
Bodil Mose Pedersen, DHI Status for implementering af ”Quality Manual”
Effectively applying ISO9001:2000 clauses 5 and 8
Key changes and transition process
An Overview of the International Quality Management Standard
University of Sunderland CIFM03Lecture 3 1 QMS / Standards CIFM03 Lecture 3.
QUALITY MANAGEMENT SYSTEM ACCORDING TO ISO
Ships in Service Training Material A-M CHAUVEL QMS Terms & Definitions 2009.
Quality Management System
1 European Conference on Training Strategies Kieran Cox -NSAI Education & Promotion-
CHAPTER 5 Infrastructure Components PART I. 2 ESGD5125 SEM II 2009/2010 Dr. Samy Abu Naser 2 Learning Objectives: To discuss: The need for SQA procedures.
Introduction to ISO New and modified requirements.
The Role of the Internal Auditor for Maintaining System Compliance and Promoting Continuous Improvement Wayne M. Uttke
Postgraduate Educational Course in radiation protection and the Safety of Radiation sources PGEC Part IV The International System of Radiation Protection.
ISO Tor Stålhane IDI / NTNU. What is ISO ISO 9001 was developed for the production industry but has a rather general structure ISO describes.
ISO 9000 and Public Awareness and Information Session 22 February 2006 Owen Glave, MBA-TQM.
ISO 9001:2000 QUALITY MANAGEMENT SYSTEM REQUIREMENTS
Software Quality Assurance Lecture 4. Lecture Outline ISO ISO 9000 Series of Standards ISO 9001: 2000 Overview ISO 9001: 2008 ISO 9003: 2004 Overview.
Lec#3 Project Quality Management Ghazala Amin. 2 Quality Specialist-Job responsibility Responsibilities Reports monitoring and measurement of processes.
Introduction to ISO 9001:2000.
TickIT Standard1 Advanced Software Engineering COM360 University of Sunderland.
ISO9001 Pre Assessment Team 10 PT Han Jian Da, Alphy Thomas Kanatt, Xia Xi, Wu Jun, May Lwin, Chit Khun, Mohit Srivastava, Kovalan Venkatesan.
1 Thank you for visiting our site and welcome to the “Introduction to ISO 22000” Presentation that you requested. For more information.
ISO 9001:2008 to ISO 9001:2015 Summary of Changes
a guidance to conversion
Paul Hardiman and Rob Brown SMMT IF Planning and organising an audit.
AET0012PPT by Dr. Anwar El-Tawil Dr. Anwar El-Tawil Director ISO Programme for Developing Countries QUALITY MANAGEMENT SYSTEM ACCORDING TO.
QUALITY MANAGEMENT STATEMENT
Exercise 1 Tor Stålhane IDI / NTNU. Intro The strength of ISO 9001 and many other standards is that they focus on “What shall be done” and leave “How.
ISO 9001:2000 The 5 Phase Plan to Implementation Sterling, VA Terry & Associates Quality.
International Security Management Standards. BS ISO/IEC 17799:2005 BS ISO/IEC 27001:2005 First edition – ISO/IEC 17799:2000 Second edition ISO/IEC 17799:2005.
It was found in 1946 in Geneva, Switzerland. its main purpose is to promote the development of international standards to facilitate the exchange of goods.
The common structure and ISO 9001:2015 additions
ISO RECORDS. ISO Environmental Management Systems2 Lesson Learning Goals At the end of this lesson you should be able to:  Describe.
Pertemuan 14 Matakuliah: A0214/Audit Sistem Informasi Tahun: 2007.
ISO 9001:2015 Subject: Quality Management System Clause 8 - Operation
Process Auditing Why do people think that this is something new? Presented by Kevin Gilson, Orion Registrar, Inc. For the ASQ ISO Users Group October 8,
1 QUALITY MANAGEMENT SYSTEM PRESENTATION TO BOTSWANA DRUG ADVISORY BOARD MEMBERS 13 th – 17 th AUGUST 2007.
WORKSHOP ON ACCREDITATION OF BODIES CERTIFYING MEDICAL DEVICES INT MARKET TOPIC 9 CH 8 ISO MEASUREMENT, ANALYSIS AND IMPROVEMENT INTERNAL AUDITS.
WORKSHOP ON ACCREDITATION OF BODIES CERTIFYING MEDICAL DEVICES INT MARKET TOPIC 6 CH 5 ISO MANAGEMENT RESPONSIBILITY Philippe Bauwin Medical.
A LOOK AT AMENDMENTS TO ISO/IEC (1999) Presented at NCSLI Conference Washington DC August 11, 2005 by Roxanne Robinson.
ISO/IEC
So where in ISO is Process?
External Validation of Quality Programs
جمهورية مصر العربية المركز القومي للبحوث التربوية والتنمية مركز معلومات و التوثيق و دعم اتخاذا القرار.
Quality Management Systems – Requirements
ISO 9000 Dr. S. Thomas Foster, Jr..
Process Auditing Why do people think that this is something new?
External Validation of Quality Programs
Nonconformity Writing
Presentation transcript:

ISO 9001 – an overview Tor Stålhane IDI / NTNU

ISO 9001 and software development ISO 9001 is a general standard – equally applicable to software development and cooking. The standard originated in the production industry. In order to simplify the introduction of ISO 9001 to software development, ISO has developed a guide – ISO This is, however, not a standard

The main part The standard ISO 9001 has five main parts. In this part of the course, we will focus on the first four of them. Quality management – part 4 Management responsibility – part 5 QA resources – part 6 Product realization – part 7 Measurement, analysis and improvement – part 8

Quality management Establish, document, implement and maintain a quality system Requirements for –what the quality system shall contain – not how things should be done –development and maintenance of a quality manual –control over the documents specified in the quality system

Management responsibility - 1 First and foremost – quality is the management’s responsibility. Management shall show that they take QA seriously. This goes for both introduction and maintenance of the quality system make sure that the QA system is adapted to the needs of the company One person in the management shall have responsibility for everything pertaining to QA.

Management responsibility - 2 Management shall periodically check how the QA system function. Important input is Reviews of the QA system Feedback from the customers Status on preventive and corrective actions Changes that may influence the QA system Suggested improvements in general

QA resources The organization shall Make available the resources needed to implement the QA system Have an overview over the need for competence and provide the training necessary Provide the infrastructure such as office space, equipment and services that are needed to make products that satisfies all requirements

Product realization - 1 The organization shall plan and develop a process for product realization. The process shall take into considerations Quality goals The needs for validation and verification The needs for proof of conformance

Product realization - 2 The organization shall identify Explicit and implicit customer requirements Requirements related to laws and regulations Organizational specific requirements, such as requirements pertaining to reuse and documentation

Product realization - 3 The organization shall evaluate all requirements before they sign a contract for development and delivery. The evaluation shall ensure that All requirements are defined All problems and TBDs are solved The organization will be able to fulfill all requirements

Product realization - 4 The organization shall establish communication channels with the customer pertaining to Product information Contract questions and problems Feedback – e.g. complaints - from the customer

Product realization - 5 The organization shall plan and design the product. This includes plans for Design and development Inspection, verification and validation Communication between those who make the design and those who do the development in order to establish a clear line of responsibility. The plan shall be updated during the project as needed.

Product realization - 6 Input to the requirements phase shall, in addition to the customer’s requirements, also include Government rules and regulations Experience from earlier, similar projects Output from design and development shall be documented in such a way that verification and validation against input is simple to perform.

Product realization - 7 We shall perform inspections and reviews according to plan. This is necessary to check that we have met all requirements for –Design and development – have worked as promised –Product – delivered as promised The organization shall control that all products that we buy from a third party are according to our requirements

Product realization - 8 If we identify process steps where we cannot verify the results based on measurement or control, these steps need to be re-validated. The validation shall show that the process step can achieve the planned / specified results.

Proof of conformance - 1 Proof of conformance – PoC – is a problem for many companies that want to be ISO certified. The purpose of PoC is to prove that we have followed the defined processes PoC has no value for the company – it is only needed for the audits It will always be a matter of opinion what should be accepted as PoC

Proof of conformance - 2 The problem with PoC is that it do not give the companies anything of value – it is just an extra cost. This creates a negative attitude towards QA plans and against QA in general. We should carefully assess how much extra work we will give the company here. It must Be sufficient to satisfy the auditors Not be so much that it creates strong negative attitudes among the developers

Proof of conformance - 3 As an example, we will consider some PoCs for the activity “Update project risk analysis”. Meeting minutes – OK Meeting plan or agenda – not so OK The risk plan is updated on the right date according to the project plan – OK but not alone