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An iso 9001 quality management system (qms) standard is one of the most widely known standards, which was introduced in 1987 and implemented in 162 countries. The iso 9001 standard has become the international reference for an organization of any size or any sector to demonstrate their ability and expertise to perform.

The iso 14001 environmental management systems (ems) certification enables you to demonstrate your commitment to the environment. The standard provides guidance on how to manage the environmental aspects of your business activities more effectively, while taking into consideration environmental protection, pollution prevention and socio-economic needs.

The iso 14001 environmental management systems (ems) certification enables you to demonstrate your commitment to the environment. The standard provides guidance on how to manage the environmental aspects of your business activities more effectively, while taking into consideration environmental protection, pollution prevention and socio-economic needs.

Organizations can INTEGRATE ISO 900114001180012200027000 Standards as per their requirements. All organizations are under pressure to demonstrate management systems that satisfy various stakeholder demands. Quality, environmental, IT security and health and safety concerns are just some of the requirements your business has to comply with today.With an integrated system, your organization becomes a unified whole, with each function aligned behind a single goal: improving the performance of the entire organization. An integrated system provides a clear, holistic picture of all aspects of your organization, how they affect each other, and their associated risks. There is less duplication, and it becomes easier to adopt new systems in future.

Isots 16949 is the international quality management standard specifically intended for organizations in the automotive industry supply community. It is for organizations that produce and deliver parts, sub-assemblies, process materials, and certain other products and services to oem manufacturing locations. Isots 16949 actually consists of iso 9001 (2008), word for word - plus a large number of automotive industry specific requirements. There are approximately 1, 039 separate and specific requirements in the basic isots 16949 standard.

The purpose of this international standard is to enable organizations to establish the systems and processes necessary to improve energy performance, including energy efficiency, use, and consumption. Implementation of this standard is intended to lead to reductions in greenhouse gas emissions, energy cost, and other related environmental impacts, through systematic management of energy. This international standard is applicable to all types and sizes of organizations irrespective of geographical, cultural or social conditions. Successful implementation depends on commitment from all levels and functions of the organization, and especially from top management.

Iso 13485:2003 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical devices and related services.the primary objective of iso 13485:2003 is to facilitate harmonized medical device regulatory requirements for quality management systems. As a result, it includes some particular requirements for medical devices and excludes some of the requirements of iso 9001 that are not appropriate as regulatory requirements. Because of these exclusions, organizations whose quality management systems conform to this international standard cannot claim conformity to iso 9001 unless their quality management systems conform to all the requirements of iso 9001.all requirements of iso 13485:2003 are specific to organizations providing medical devices, regardless of the type or size of the organization.

Hazard analysis and critical control point (haccp) iso 22000 food safety management system is a process control system designed to identify and prevent microbial and other hazards in food production and entire food chain. Haccp includes steps designed to prevent problems before they occur and to correct deviations through a systematic way as soon as they are detected. Such preventive control systems with documentation and verification are widely recognized by scientific authorities and international organizations as the most effective approach available for producing safe food. Haccp iso 22000 enables the producers, processors, distributors, exporters, etc, of food products to utilize technical resources efficiently and in a cost effective manner in assuring food safety. The iso 22000:2005 standard outlines food safety management system requirements for any organization in the food chain, and is one of a family of standards focused at the development, implementation and improvement of a food safety management system.

Halal simply means permitted or lawful. So when we are talking about halal foods it means any foods that are allowed to be eaten according to islamic sharia law. This means that for any food to be considered halal it must comply with the religious ritual and observance of sharia law. This means that halal certificate ensures that food has been subjected to approved certification systems which guarantee to consumers that nothing in the food has any forbidden components.

The BRC Global Standards are a leading global safety and quality certification programme, used throughout the world by over 17, 000 certificated suppliers in 90 countries through a network of over 80 accredited and BRC recognised Certification Bodies. The BRC Global Standards are widely used by suppliers and global retailers. They facilitate standardization of quality, safety, operational criteria and manufacturers’ fulfillment of legal obligations. They also help provide protection to the consumer.

Kosher foods are those that conform to the regulations of the jewish halakhic law framework, kosher meaning fit or allowed to be eaten only by the halakhic community. A list of some kosher foods are found in the book of leviticus 11:1-47. There are also certain kosher rules found there. Reasons for food not being kosher include the presence of ingredients derived from nonkosher animals or from kosher animals that were not slaughtered in the ritually proper manner, a mixture of meat and milk, or grape juice (or their derivatives) produced without supervision, the use of produce from israel that has not been tithed, or the use of non-kosher cooking utensils and machinery.

Globalg.a.p. Is a private sector body that sets voluntary standards for the certification of production processes of agricultural (including aquaculture) products around the globe. The globalg.a.p. Standard is primarily designed to reassure consumers about how food is produced on the farm by minimizing detrimental environmental impacts of farming operations, reducing the use of chemical inputs and ensuring a responsible approach to worker health and safety as well as animal welfare.

An information security management system (isms) is a management system based on a systematic business risk approach, to establish, implement, operate, monitor, review, maintain, and improve information security. It is an organizational approach to information security. Isoiec 27001 (bs 7799) is a standard for information security that focuses on an organization’s isms.

isoiec 17025:2005 specifies the general requirements for the competence to carry out tests andor calibrations, including sampling. it covers testing and calibration performed using standard methods, non-standard methods, and laboratory-developed methods.it is applicable to all organizations performing tests andor calibrations. these include, for example, first-, second- and third-party laboratories, and laboratories where testing andor calibration forms part of inspection and product certification.

Iso 30000:2008 specifies requirements for a management system to enable a ship recycling facility to develop and implement procedures, policies and objectives in order to be able to undertake safe and environmentally sound ship recycling operations in accordance with national and international standards. The management system requirements take into account the relevant legal requirements, safety standards and environmental elements that the ship recycling facility needs to identify and comply with in order to carry out safe and environmentally sound ship recycling. Iso 30000:2008 applies to the entire process: accepting a ship for recycling by the facility; assessing the hazards onboard the ship; identifying and complying with any applicable notification and import requirements for ships to be recycled; carrying out the recycling process in a safe and environmentally sound manner; conducting required training; ensuring the availability of social amenities (e.g. First aid, health checks, food and beverages); storage and processing of materials and wastes from the ship; waste stream and recycling stream management, including contractual agreements; and documentation controls for the process, including any applicable notification of the final disposal of the vessel.

Sa 8000 is an international certification standard that encourages organizations to develop, maintain and apply socially acceptable practices in the workplace. With a steady rise in the number of corporate scandals, companies recognize the need to consider the effects their activities and policies can have on their reputation and credibility in the marketplace. Companies need to consider the social impact of their operations, in addition to the conditions under which employees, partners and suppliers operate. This means controlling and practicing respect and promotion of human rights for all employees throughout the whole supply, production and distribution chain.

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Six Sigma at many organizations simply means a measure of quality that strives for near perfection. Six Sigma is a disciplined, data-driven approach and methodology for eliminating defects (driving toward six standard deviations between the mean and the nearest specification limit) in any process – from manufacturing to transactional and from product to service..

The CE marking is a key indicator of a product's compliance with EU legislation and enables the free movement of products within the European market. By affixing the CE marking on a product, a manufacturer is declaring, at their sole responsibility, conformity with all of the legal requirements to achieve CE marking and therefore ensuring validity for that product to be sold throughout the European Economic Area. This also applies to products made in third countries which are sold in the EEA.CE marking does not indicate that a product was made in the EEA but states only that the product has been assessed before being placed on the market and thus satisfies the legislative requirements (e.g. a harmonized level of safety) to be sold there. It means that the manufacturer has verified that the product complies with all relevant essential requirements (such as safety, health, environmental protection requirements) of the applicable directive(s) or, if stipulated in the directive(s), has had it examined by a notified conformity assessment body. However, not all products must bear the CE marking. Only those product categories subject to specific directives that provide for the CE marking are required to be CE-marked. CE-marked products are bought not only by professionals (e.g. medical devices, lifts, machinery and measuring equipment) but also by consumers (e.g. toys, PCs, mobile phones and light bulbs).

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