KISII UNIVERSITY
COLLEGE
GROUP FOURTEEN
(G14)
COURSE TOTAL QUALITY MANAGEMENT
CODE BCOM/BBAM 472
FACULTY COMMERCE
TASK INTERNATIONAL
STANDARDS ORGANISATION
INSTRUCTOR MRS. ODERO EUCABETH
GROUP
MEMBERS
1.
MUYALE
MAXWEL KISIENYA C12/60291/08
2.
OGONGO
GEOFFREY OGEKE C12/60256/08
3.
WILSON
EPHLON NYACHWAYA C12/60295/08
4.
GETRUDE
MAPENZI C11/60206/08
5.
PHYLIS
NJUGUNA
C11/60170/08
6.
JOHN
GIOKO MUTHOMI C12/60895/07
7.
KELVIN
KUBAI C12/60281/08
8.
SIONGOK FRED C12/60307/08
Q.
1 Discuss ISO 9000 Quality system and describe ISO 9000 series of standards?
INTRODUCTION
ISO (International Organization for
Standardization) is the world's largest
developer and publisher of International
Standards.ISO is a network
of the national standards institutes of 161
countries, one member per country, with a Central Secretariat in Geneva,
Switzerland, that coordinates the system.
ISO is a non-governmental organization that forms a bridge between the
public and private sectors. On the one hand, many of its member institutes are
part of the governmental structure of their countries, or are mandated by their
government. On the other hand, other members have their roots uniquely in the
private sector, having been set up by national partnerships of industry
associations.
Therefore, ISO enables a consensus to be reached on solutions
that meet both the requirements of business and the broader needs of society.
FUNCTIONS OF ISO
·
Make the development, manufacturing
and supply of products and services more
efficient, safer and cleaner.
·
Facilitate
trade between countries and make it fairer.
·
Provide governments with a technical
base for health, safety and
environmental legislation, and conformity assessment.
·
Share
technological advances and good management practice.
·
Disseminate innovation.
·
Safeguard consumers
and users in general, of products and services.
·
Make life simpler by providing solutions to common problems.
What
is ISO 9000?
ISO 9000
is a generic name given to a family
of standards
developed to provide a framework around which a quality management system can
effectively be implemented.
International
Organization for Standardization evolved ISO 9000 series of standards in 1987.
These are quality assurance system standards. First revision came in July 1994
and second revision on Dec 15, 2000. Henceforth, there will be only one
standard ISO-9001:2000.
These
standards are customer oriented and focus on customer satisfaction by
fulfilling the customers’ requirements.
These
are applicable to any manufacturing or servicing organization. Hence, these are
the product neutral standards.
These
standards can be adopted by any organization -be it large, medium, small;
limited company, private limited company, partnership firms, and proprietorship
firms.
ISO 9001:2000, the requirement
standard, includes the following main sections:
Quality Management System
Management Responsibility
Resource Management
Product Realization
Measurement Analysis and Improvement
In this
competitive era, especially when liberalization, privatization and
globalization (LPG) concepts are taking deep roots, survival of the
organization will be at stake if outdated systems and procedures are followed.
Hence, there is a need to have the systems- based approach in all business
functions to meet the cost effective quality and timely delivery requirements.
It is
quite likely that in future many organizations will act as subcontractors to
the major global players. In such situation, the adoption of ISO 9000 quality
systems and its certified performance would help in establishing credentials
and capability of an organization to get the contracts.
It is
therefore aptly said "one cannot do today’s work with yesterday’s methods
and still be in the business tomorrow".
Quality
management principles
There
are eight quality management principles on which the quality management system
standards of the ISO 9000:2000 and ISO 9000:2008 series are based. These
principles can be used by senior management as a framework to guide their
organizations towards improved performance. The principles are derived from the
collective experience and knowledge of the international experts who
participate in ISO Technical Committee ISO/TC 176, Quality management
and quality assurance, which is responsible for
developing and maintaining the ISO 9000 standards.
The
eight quality management principles are defined in ISO 9000:2005, Quality
management systems Fundamentals and vocabulary, and in ISO 9004:2000, Quality
management systems Guidelines for performance improvements.
This
document gives the standardized descriptions of the principles as they appear
in ISO 9000:2005 and ISO 9004:2000. In addition, it provides examples of the
benefits derived from their use and of actions that managers typically take in
applying the principles to improve their organizations' performance.
ISO 9000 Series of Standards
ISO is responsible for the promotion and
development of international standards and related activities, including
conformity assessments such as testing, inspection, laboratory accreditation,
certification and quality assessments.
The ISO 9000 series standards have
been adopted by more than 45 countries and its equivalent standard in the
Indian context is the Bureau of Indian Standards' (BIS) 14000 series. In the
United States, the series is known as the ANSI/ASQC Q 9000 series.
The standard finds its origin in the
European Community (EC) July 1985 product liability directives (also known as
the single market directives) which state that for certain regulated products,
manufacturers exporting to the EC and, eventually, to the European Free Trade
Association, would need to have a well documented and implemented Quality
Assurance System.
The ISO 9000 series standards
provide the requirements to which organizations desirous of certification must
conform. One very important aspect of the standards is that they were very
generic in nature and ingenuity is required while interpreting the standards'
applicability to the industry or firm in question.
Developed by the ISO Technical
Committee 176, published in 1987 and updated approximately every five years,
the standards comprise five documents whose focus is Quality Assurance Systems.
These five documents are:
a) ISO 9000 -
Quality Management and Quality Assurance Standards - Guidelines for selection and use
Quality Management and Quality Assurance Standards - Guidelines for selection and use
b) ISO 9001 -
Quality systems - Model for quality assurance in design, production, installation and servicing. This is the most comprehensive standard with 20 clauses.
Quality systems - Model for quality assurance in design, production, installation and servicing. This is the most comprehensive standard with 20 clauses.
c) ISO 9002 -
Quality systems - model for quality assurance in production and installation. This standard has 18 clauses.
Quality systems - model for quality assurance in production and installation. This standard has 18 clauses.
d) ISO 9003 -
Quality systems - Model for quality assurance in final inspection and test. Requires conformity with 12 clauses.
Quality systems - Model for quality assurance in final inspection and test. Requires conformity with 12 clauses.
e) Quality management and quality
system elements - Guidelines.
Q.2 What are the benefits that organizations
can accrue on implementing ISO 9000?
Organizations that adopt to implement the
quality management system are expected to apply the principles of ISO 9000 from
which each comes with different benefits.
These benefits are discussed under each
principle:
Principle 1:
Customer focus
Organizations
depend on their customers and therefore should understand current and future
customer needs, should meet customer requirements and strive to exceed customer
expectations.
- Increased revenue and market share obtained through flexible and fast responses to market opportunities.
- Increased effectiveness in the use of the organization's resources to enhance customer satisfaction.
- Improved customer loyalty leading to repeat business.
Principle 2:
Leadership
Leaders establish
unity of purpose and direction of the organization. They should create and
maintain the internal environment in which people can become fully involved in
achieving the organization's objectives.
- People will understand and be motivated towards the organization's goals and objectives.
- Activities are evaluated, aligned and implemented in a unified way.
- Miscommunication between levels of an organization will be minimized.
Principle 3:
Involvement of people
People at
all levels are the essence of an organization and their full involvement
enables their abilities to be used for the organization's benefit.
- Motivated, committed and involved people within the organization.
- Innovation and creativity in furthering the organization's objectives.
- People being accountable for their own performance.
- People eager to participate in and contribute to continual improvement.
Principle 4:
Process approach
A desired
result is achieved more efficiently when activities and related resources are
managed as a process.
- Lower costs and shorter cycle times through effective use of resources.
- Improved, consistent and predictable results.
- Focused and prioritized improvement opportunities.
Principle 5:
System approach to management
Identifying,
understanding and managing interrelated processes as a system contributes to
the organization's effectiveness and efficiency in achieving its objectives.
- Integration and alignment of the processes that will best achieve the desired results.
- Ability to focus effort on the key processes.
- Providing confidence to interested parties as to the consistency, effectiveness and efficiency of the organization.
Principle 6:
Continual improvement
Continual
improvement of the organization's overall performance should be a permanent
objective of the organization.
- Performance advantage through improved organizational capabilities.
- Alignment of improvement activities at all levels to an organization's strategic intent.
- Flexibility to react quickly to opportunities.
Principle 7:
Factual approach to decision making
Effective
decisions are based on the analysis of data and information
- Informed decisions.
- An increased ability to demonstrate the effectiveness of past decisions through reference to factual records.
- Increased ability to review, challenge and change opinions and decisions.
Principle 8:
Mutually beneficial supplier relationships
An
organization and its suppliers are interdependent and a mutually beneficial
relationship enhances the ability of both to create value
- Increased ability to create value for both parties.
- Flexibility and speed of joint responses to changing market or customer needs and expectations.
- Optimization of costs and resources.
PRACTICAL
EXAMPLES
Standardization of screw threads helps to keep chairs,
children's bicycles and aircraft together and solves the repair and
maintenance problems caused by a lack of standardization that were
once a major headache for manufacturers and product users.
Standards establishing an international consensus on terminology
make technology transfer easier and safer. They are an important stage in the
advancement of new technologies and dissemination of innovation.
Without the standardized dimensions of
freight containers, international trade would be slower and more expensive.
Without the standardization of telephone and banking
cards, life would be more complicated.
A lack of standardization may even affect the
quality of life itself: for the disabled, for
example, when they are barred access to consumer products, public transport and
buildings because the dimensions of wheel-chairs and entrances are not
standardized.
Standardized symbols provide danger
warnings and information across linguistic frontiers.
Consensus
on grades of various materials gives a common reference for
suppliers and clients in business dealings.
Agreement
on a sufficient number of variations of a product to meet most current
applications allows economies of scale with cost
benefits for both producers and consumers. An example is the
standardization of paper sizes.
Standardization
of performance or safety requirements of diverse equipment
makes sure that users' needs are met while allowing individual manufacturers
the freedom to design their own solution on how to meet those needs.
Standardized
computer protocols allow products from different vendors to
"talk" to each other.
Standardized
documents speed up the transit of goods, or identify sensitive
or dangerous cargoes that may be handled by people speaking different
languages.
Standardization
of connections and interfaces of all types ensures the compatibility
of equipment of diverse origins and the interoperability of
different technologies.
Agreement
on test methods allows meaningful comparisons of products, or
plays an important part in controlling pollution - whether by
noise, vibration or emissions.
Safety
standards for machinery protect people at work, at play, at
sea... and at the dentist's.
Without
the international agreement contained in ISO standards on metric
quantities and units, shopping and trade would be haphazard, science
would be unscientific and technological development would be handicapped.
Discuss
the requirements of ISO 9001:2008
Document: ISO/TC 176/SC 2/N525R2
October 2008
October 2008
Introduction
Two of
the most important objectives in the revision of the ISO 9000 series of
standards have been
to
develop a simplified set of standards that will be equally applicable to
small as well as medium and large organizations, and
for the
amount and detail of documentation required to be more relevant to the desired
results of the organization’s process activities.
ISO 9001:2008, Quality management
systems – Requirements has
achieved these objectives, and the purpose of this additional guidance is to
explain the intent of the new standard with specific regard to documentation.
ISO
9001:2008 allows an organization flexibility in the way it chooses to document
its quality management system (QMS). This enables each individual organization
to develop the minimum amount of documentation needed in order to demonstrate
the effective planning, operation and control of its processes and the
implementation and continual improvement of the effectiveness of its QMS.
It is
stressed that ISO 9001 requires (and always has required) a “Documented
quality management system”, and not a “system of documents”.
The
following are some of the main objectives of an organization’s documentation,
independent of whether or not it has implemented a formal QMS;
a)
Communication of Information
As a
tool for information transmission and communication. The type and extent of the
documentation will depend on the nature of the organization’s products and
processes, the degree of formality of communication systems and the level of
communication skills within the organization, and the organizational culture.
b)
Evidence of conformity -Provision of evidence that what was
planned, has actually been done.
c)
Knowledge sharing -To disseminate and preserve the
organization’s experiences. A typical example would be a technical
specification, which can be used as a base for design and development of a new
product.
ISO 9001:2008
Documentation Requirements
ISO
9001:2008 clause 4.1 General requirements requires an organization to
“establish, document, implement, and maintain a quality management
system and continually improve its effectiveness in accordance with the
requirements of this International Standard”
Clause
4.2.1 General explains that the quality management system
documentation shall include:
ü
Documented
statements of a quality policy and quality objectives;
ü
A
quality manual
ü
Documented
procedures required by this International Standard
ü
Documents
needed by the organization to ensure the effective planning, operation
and control of its processes, and
ü
Records
required by this International Standard;
The
notes after Clause 4.2 make it clear that where the standard specifically
requires a “documented procedure”, the procedure has to be established,
documented, implemented and maintained. It also emphasizes that the extent of
the QMS documentation may differ from one organization to another due to:
§
the
size of organization and type of activities;
§
the
complexity of processes and their interactions, and
§
the
competence of personnel.
All the
documents that form part of the QMS have to be controlled in accordance with
clause 4.2.3 of ISO 9001:2008, or, for the particular case of records,
according to clause 4.2.4.
Guidance on Clause 4.2 of ISO 9001:2008
The
following comments are intended to assist users of ISO 9001:2008 in
understanding the intent of the general documentation requirements of the
International Standard.
a) Documented
statements of a quality policy and objectives:
Requirements
for the quality policy are defined in clause 5.3 of ISO 9001:2008. The
documented quality policy has to be controlled according to the requirements of
clause 4.2.3.
Note: Organizations that are revising their quality policy for the first time, or in order to meet the amended requirements in ISO 9001:2008, should pay particular attention to clause 4.2.3 (c), (d) and (g).
Note: Organizations that are revising their quality policy for the first time, or in order to meet the amended requirements in ISO 9001:2008, should pay particular attention to clause 4.2.3 (c), (d) and (g).
Requirements
for quality objectives are defined in clause 5.4.1 of ISO 9001:2008. These
documented quality objectives are also subject to the document control
requirements of clause 4.2.3.
b) Quality
Manual:
Clause
4.2.2 of ISO 9001:2008 specifies the minimum content for a quality manual. The
format and structure of the manual is a decision for each organization, and
will depend on the organization’s size, culture and complexity. Some
organizations may choose to use the quality manual for other purposes besides
that of simply documenting the QMS
A small
organization may find it appropriate to include the description of its entire
QMS within a single manual, including all the documented procedures required by
the standard.
Large,
multi-national organizations may need several manuals at the global, national
or regional level, and a more complex hierarchy of documentation.
The
quality manual is a document that has to be controlled in accordance with the
requirements of clause 4.2.3.
c) Documented
procedures:
ISO
9001:2008 specifically requires the organization to have “documented
procedures” for the following six activities:
4.2.3 Control of documents
4.2.4 Control of records
8.2.2 Internal audit
8.3 Control of nonconforming product
8.5.2 Corrective action
8.5.3 Preventive action
4.2.3 Control of documents
4.2.4 Control of records
8.2.2 Internal audit
8.3 Control of nonconforming product
8.5.2 Corrective action
8.5.3 Preventive action
These
documented procedures have to be controlled in accordance with the requirements
of clause 4.2.3
Some
organizations may find it convenient to combine the procedure for several
activities into a single documented procedure (for example, corrective action
and preventive action). Others may choose to document a given activity by using
more than one documented procedure (for example, internal audits). Both are
acceptable.
Some
organizations (particularly larger organizations, or those with more complex
processes) may require additional documented procedures (particularly those
relating to product realization processes) to implement an effective QMS.
Other
organizations may require additional procedures, but the size and/or culture of
the organization could enable these to be effectively implemented without
necessarily being documented. However, in order to demonstrate compliance with
ISO 9001:2008, the organization has to be able to provide objective evidence
(not necessarily documented) that its QMS has been effectively implemented.
d) Documents
needed by the organization to ensure the effective planning, operation and
control of its processes:
In order
for an organization to demonstrate the effective implementation of its QMS, it
may be necessary to develop documents other than documented procedures.
However, the only documents specifically mentioned in ISO 9001:2008 are:
- Quality policy (clause 4.2.1.a)
- Quality objectives (clause 4.2.1.a)
- Quality manual (clause 4.2.1.b)
- Quality policy (clause 4.2.1.a)
- Quality objectives (clause 4.2.1.a)
- Quality manual (clause 4.2.1.b)
There
are several requirements of ISO 9001:2008 where an organization could add value
to its QMS and demonstrate conformity by the preparation of other documents,
even though the standard does not specifically require them. Examples may
include:
- Process maps, process flow charts and/or process descriptions
- Organization charts
- Specifications
- Work and/or test instructions
- Documents containing internal communications
- Production schedules
- Approved supplier lists
- Test and inspection plans
- Quality plans
- Process maps, process flow charts and/or process descriptions
- Organization charts
- Specifications
- Work and/or test instructions
- Documents containing internal communications
- Production schedules
- Approved supplier lists
- Test and inspection plans
- Quality plans
All such
documents have to be controlled in accordance with the requirements of clause
4.2.3 and/or 4.2.4, as applicable
e) Records:
Organizations
are free to develop other records that may be needed to demonstrate conformity
of their processes, products and quality management system.
Requirements
for the control of records are different from those for other documents, and
all records have to be controlled according to those of clause 4.2.4 of ISO
9001:2008.
REFERENCE
1. Feigenbaum, A.V.: Total Quality Control.
McGraw-Hill, 3rd edition, New
York, USA, 1991
2. Garvin, D.A.: Competing on the eight dimensions
of quality.
3. Harvard Business Review, Nov./Dec., 1987
4. ISO 9001 requirements summary
5. ISO 9000 ,
BSI Group, 389 Chiswick High Road, London,
7. www.isoquirements.com
The caliber of information that you're offering is merely wonderful.Connie Smith
ReplyDeleteThank for sharing information for ISO STandard. This is helpful to know the system of quality management ISO Certification.
ReplyDeleteThose rules moreover attempted to wind up plainly a decent approach to perceive that other individuals online have the indistinguishable enthusiasm like mine to get a handle on incredible arrangement more around this condition.
ReplyDeletefire and safety course in chennai
I ‘d mention that most of us visitors are endowed to exist in a fabulous place with very many wonderful individuals with very helpful things.
ReplyDeleteindustrial safety course in chennai
You were very interesting.. But sadly I didnrrrt accept them much :/ Although I may disagree I still support you as how confident happen to be on your writing lol AMREP Mexico
ReplyDeleteThis comment has been removed by the author.
ReplyDeleteThank you a lot for providing individuals with a very spectacular possibility to read critical reviews from this site.top 10 audit firms dubai
ReplyDeletenice share! thanks for the post..
ReplyDeleteI agree with all of you that this information is pretty useful which definitely deserve
ReplyDeletefor bookmark.
EMS Certification Services
Thank you for bringing to a halt my long search topic. I really benefited from your content.
ReplyDeleteISO Lead Auditor Course Online
Nice Post and liked it
ReplyDeleteTo know more about How will ISO certification benefit my organization, please visit
How will ISO certification benefit my organization
Nice post. I learn something totally new and challenging on sites . It's always helpful to read content..
ReplyDeleteISO Certification
Thanks for give me this information really this product is very effective.
ReplyDeleteiso 27001 consultant singapore
very informative a thank you for posting
ReplyDeleteISO 9001 Certification
Good day. I was impressed with your article. Keep it up . You can also visit my site if you have time. Thank you and Bless you always.
ReplyDeleteiso 14001 training in hong kong
This is really an awesome article. Thank you for sharing this.It is worth reading for everyone.
ReplyDeletefda registration
This post is really nice and informative. The explanation given is really comprehensive and informative..
ReplyDeleteISO 15189 Certification
Good day. I was impressed with your article. Keep it up . You can also visit my site if you have time. Thank you and Bless you always.
ReplyDeleteISO training hong kong
Nice
ReplyDeleteeducational tablet
Very Nice. This blog is very useful to me.
ReplyDeleteISO certification
International Standards I have read all the comments and suggestions posted by the visitors for this article are very fine,We will wait for your next article so only.Thanks!
ReplyDeletenice post.
ReplyDeleteiso 15189 internal auditor course
The ISO 45001 training in Pakistan empowers participants to comprehend occupational health and safety, compliance, auditing, consultancy, and risk management and cultivate a safer working environment in industries or office spaces for employees.
ReplyDeleteThank you for sharing your information and your site or blog this is simple but nice Information I’ve ever seen i like it i learn something today.
ReplyDeletecertification of quality management system near me
Finding best Chronic Pain Clinic Orangeville? So New Hope provide complete Chronic Pain treatment support and advice on varied measures. Chronic Pain Clinic Orangeville
ReplyDeleteContact Us: Phone: 519-217-9300 Email: admin@newhopephysio.com Web: www.newhopephysio.com