ISO Standards
Optimizing on our team of industry experts, sector
specific knowledge and with the rudimentary understanding of our clients'
requirements, We offer customized solutions for certification &
consulting in India, UAE, South East Asia, Middle East, Europe, USA for ISO
9001 Consultancy & Certification, ISO 14001 certification consultancy,
OHSAS 18001 certification consultancy, ISO/TS 16949:2002 certification, ISO
22000 certification consultancy, ISO 27001 certification consultancy &
ISO 13485 certification consultancy to maximize functionality of processes
and add value to client’s business. We offer consultancy &
certification solutions to our client companies for the following ISO
certification and other quality certification standards:-
In ISO 9001 Certification, highly competent market
industries with ISO 9001 2000 certification hold a distinguished position.
These industries hold an advantage over others and have gained trust &
credibility. The ISO 9001:2000 quality certification is based on the
following eight fundamental quality management principles:
- Customer focus
- Leadership
- Involvement of people
- Process approach
- System approach to management
- Continual improvement
- Factual approach to decision making
- Mutually beneficial supplier relationships
Overview of the ISO 9001:2000 standard
ISO 9001:2000 contains five requirements sections, each dealing with one of
the fundamental building blocks required by any process. These are:
Quality Management System: This section details the general and
documentation requirements that are the foundation of the management system.
The general requirements ask you to look at the processes of the management
system, how they interact with each other, what resources you need to run
the processes; and how you will measure and monitor the processes. The
second part of the section then sets out the requirements for the
documentation needed to effectively operate the system and how the
documentation should be controlled.
Management Responsibility: The management of the systems is the
responsibility of the "top management" at a strategic level in the
organization. The "top management" must know customers'
requirements at a strategic level and make a commitment to meeting these as
well as statutory and regulatory requirements. "Top management"
must also set policies; and to achieve these policies set objectives through
planning how the objectives will be met. "Top management" should
also ensure that there are clear internal communications and that the
management system is regularly reviewed.
Resource Management: This covers the people and physical resources
needed to carry out the processes. People should be competent to carry out
their tasks and the physical resources and work environment need to be
capable of ensuring that the customers' requirements are met.
Product/Service realization: These are the processes necessary to
produce the product or to provide the service. This is the act of converting
the input of the process to the output. For a manufacturing organization,
this may be the process of converting iron ore to steel via a blast furnace
for example. For a service organization, this may be the process of moving a
product or person from one place to another, for example, a taxi journey.
Measurement analysis and improvement: These are the measurements to
enable the systems to be monitored to provide information on how the systems
are performing with respect to the customer, the management systems
themselves through internal audits, the processes and the product. Analyzing
these, including any defect or shortfall in performance, will provide
valuable information for use in improving the systems and products where
this is required.
Each of these five fundamental building blocks is required for any process
because, if one is missing, a controlled process does not occur.
The advantages of being ISO 9001:2000 compliance : - : -
1. Improved outcome of process
2. Professional image
3. Increased customer confidence
4. Better marketability
5. Clarity of responsibility and authority
6. Better and defined system
7. Consistent Quality
Compliance with ISO 14000 certification series highlights
adherence with environmental management standards developed by the
International Organization for Standardization (ISO). ISO one of the world's
principal voluntary standards development bodies. The ISO 14000
certification standards are designed to provide an internationally
recognized framework for environmental management, measurement, evaluation
and auditing.
International Standards- ISO 14001:2004 intended to provide
organizations with the elements of an effective environmental management
system (EMS) that can be integrated with other management requirements and
help organizations to achieve environmental and economic goals
This International Standard specifies requirements for an environmental
management system to enable an organization to develop and implement a
policy and objectives which take into account legal requirements and
information about significant environmental aspects. It is intended to apply
to all types and sizes of organization and to accommodate diverse
geographical, cultural and social conditions. The overall aim of this
International Standard is to support environmental protection and prevention
of pollution in balance with socio-economic needs.
This International Standard is based on the methodology known as
Plan-Do-Check-Act (PDCA). PDCA can be briefly described as follows.
Plan: establish the objectives and processes necessary to deliver results
in accordance with the organization's environmental policy.
Do: implement the processes.
Check: monitor and measure processes against environmental policy,
objectives, targets, legal and other requirements, and report the results.
Act: take actions to continually improve performance of the
environmental management system
To achieve ISO 14001 organisation requires followings :
- Establish an appropriate environmental policy.
- Identify the environmental aspects arising from the organizations
past, existing or planned activities, products and services, in order to
determine the environmental impacts of significance.
- Identify applicable legal requirements and other requirements, to
which the organization subscribes.
- Identify priorities and set appropriate environmental objectives and
targets.
- Establish a structure and a programme(s) to implement the policy and
achieve objectives and meet targets.
- Facilitate planning, control, monitoring, preventive and corrective
actions, auditing and review activities to ensure both that the policy
is complied with and that the environmental management system remains
appropriate
- Be capable of adapting to changing circumstances.
Advantages of ISO 14001:2004
1. Process improvement.
2. Environmental cost reduction.
3. Better relationships with regulators
4.Better relationships with insurers, investors, and financial markets
5.Product improvement
6. Marketing advantages
7. Better control of liabilities
8.educed regulatory burden
9.Protection of company image and name
10.emonstration of responsible management
The OHSAS 18001 is the international Occupational Health
and Safety Management System standard. These standards are applicable to
companies of any size, but is especially relevant to companies with a large
work force, manual and heavy work tasks, and/or high risk work environments.
Targeting the health and safety of employees proves that you are actively
working to ensure that your operations are safe both for your employees and
the surrounding environment.
The benefits of implementing a systematic and
effective OHSAS management system include the following:
1. Reducing the number of personnel injuries through prevention and control
of workplace hazards.
2. Reducing the risk of major accidents.
3. Ensuring a well-qualified and enthusiastic workforce by fulfillment of
the increasing expectations of your employees.
4. Reducing the material loss caused by accidents and in production
interruptions.
5. Reducing insurance costs as well as reducing costs due to absence of
employees.
6. Serving the possibility for an integrated management system including
quality, environment and health and safety.
7. Ensuring that appropriate legislation is addressed and acted upon.
8. Meeting the increasing importance of OH&S for public image.
OHSAS 18001 has been developed to be compatible with ISO 9001 and
ISO 14001 to allow for easy integration. Legislative & regulatory
commitment and continual improvement are two important aspects of OHSAS
18001.
The elements of OHSAS 18001 include:
1. Policy and commitment.
2. Hazard identification, risk assessment & risk controls.
3. Legal requirements.
4. Objectives & Programs.
5. Organization & personnel.
6. Training, Communication & Consultation.
7. Documentation & records.
8. Operational Controls.
9. Emergency Readiness.
10. Measurement & monitoring.
11. Accident & incident investigation, corrective & preventive
action.
12. Audit & Review.
This International Standard ISO 22000 specifies
requirements for a food safety management system where an organization in
the food chain needs to demonstrate its ability to control food safety
hazards in order to ensure that food is safe at the time of human
consumption.
It is applicable to all organizations, regardless of size, which are
involved in any aspect of the food chain and want to implement systems that
consistently provide safe products. The means of meeting any requirements of
this International Standard can be accomplished through the use of internal
and/or external resources.
This International Standard ISO 22000 specifies
requirements to enable an organization
- To plan, implement, operate, maintain and update a food safety
management system aimed at providing products that, according to their
intended use, are safe for the consumer
- To demonstrate compliance with applicable statutory and regulatory
food safety requirements
- To evaluate and assess customer requirements and demonstrate
conformity with those mutually agreed customer requirements that relate
to food safety, in order to enhance customer satisfaction
- To effectively communicate food safety issues to their suppliers,
customers and relevant interested parties in the food chain
- To ensure that the organization conforms to its stated food safety
policy
- To demonstrate such conformity to relevant interested parties and
- To seek certification or registration of its food safety management
system by an external organization, or make a self-assessment or
self-declaration of conformity to this International Standard.
All requirements of this International Standard (ISO 22000) are generic and
are intended to be applicable to all organizations in the food chain
regardless of size and complexity. This includes organizations directly or
indirectly involved in one or more steps of the food chain. Organizations
that are directly involved include, but are not limited to, feed producers,
harvesters, farmers, producers of ingredients, food manufacturers,
retailers, food services, catering services, organizations providing
cleaning and sanitation services, transportation, storage and distribution
services. Other organizations that are indirectly involved include, but are
not limited to, suppliers of equipment, cleaning and sanitizing agents,
packaging material, and other food contact materials.
This International Standard allows an organization, such as a small and/or
less developed organization (e.g. a small farm, a small packer-distributor,
a small retail or food service outlet), to implement an externally developed
combination of control measures.
ISO / TS 16949:2002 certification is an international
standard and "technical specification" containing requirements for
establishing and maintaining a quality management system for the design and
development, production and installation (when relevant) and service of
automobile-related products. The 20 element structure of QS 9000 and ISO /
TS 16949 : 1999 is now a thing of past. The 2002 version has adopted the
content and structure of ISO 9001 certification : 2000, which promotes a "Process
Approach" to develop, implement and improve a quality management
system.
Benefits of ISO/TS 16949
1. Fosters improved product & process quality.
2. Incorporates the best lessons learnt from the global automotive realm.
3. Provides additional confidence for global sourcing.
4. Ensures a global quality system approach in the supply chain for
supplier/subcontractor service consistency.
5. Reduces variation, waste & improves the overall efficiency in
production levels.
6. Eliminates the need for multiple third party registrations.
7. Provides a common platform to address worldwide quality system
requirements.
8. Formatted to allow easy conversion to ISO9001/2000.
9. Advantageous to the up gradation of existing quality systems.
ISO 27001, titled "Information Security Management -
Specification With Guidance for Use", is the replacement for BS7799-2.
It is intended to provide the foundation for third party audit, and is
'harmonized' with other management standards, such as ISO 9001 and ISO
14001.
The basic objective of the standard is to help establish and maintain an
effective information management system, using a continual improvement
approach. It implements OECD (Organization for Economic Cooperation and
Development) principles, governing security of information and network
systems.
The Contents of the Standard?
The broad content is of course similar to the old BS7799. Included is:
1.Cross reference with ISO 17799 controls
2.Use of PDCA
3 Information Management System
4. Tems and definitions
ISO 27001 Certification
As with BS7799-2, a robust audit and certification scheme supports the
standard. For those already certified against BS7799, accredited
certification bodies will establish transitional arrangements. More detail
and explanation is available on our specific certification page
The ISO 27000 Series
The final version of ISO 27001 was published in October 2005 to a great
fanfare. It should be noted, however, that this is in fact only the first of
a series of standards to support information security. Having stated this,
it may well be the most important, at least from a 'top down' perspective,
as it defines the information security management system.
ISO 13485:2003 Quality
Management System
ISO 13485 is an international standard that specifies
requirements for a quality management system that can be used by an
organization for the design and development, production, installation, and
servicing of medical devices. This standard can also be used by
international and external parties, including certification bodies, for
assessment of the organization's ability to meet customer and regulatory
requirements. The quality management system requirements specified in the
ISO 13485:2003 standard complements technical requirements for products. The
primary purpose of the ISO 13485:2003 standard is to facilitate harmonized
medical device regulatory requirements for quality systems. All requirements
of the ISO 13485:2003 standard are specific to organizations providing
medical devices, regardless of the type or size.
Contact Us for value added, Cost effective, Time Bound and Result Oriented
ISO Consultancy & Certification in India, USA, UK, Middle East, UAE,
Saudi Arabia, Oman, Qatar, Kuwait, Yemen, Bahrain, Jordon, Turkey, Maldives,
Greece, Europe, Africa, South East Asia, Singapore, Malaysia, Thailand,
Indonesia, Sri Lanka, Bangladesh and Nepal.