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ISO 9001:2015
ISO 9001: 2015 defines quality as ‘the degree to which a set of inherent characteristics fulfills requirements.’ Grade denotes a category or grade attributed to a product, and grades and categories of products having the same functional use can be widely different. The term quality assurance is used to denote actions that lead to building confidence in all concerned stakeholders that requirements would be fulfilled. The term quality control simply focuses on fulfilling quality requirements. Quality management, on the other hand, encompasses all activities, maintaining the focus on distinction and control aspects in an organization as regards quality is concerned. Gaining competitive advantage through quality; Successful companies are those driven by quality- from the way they operate, to the customer service standards they set and the products they deliver. Focusing on quality makes for leaner, fitter organization, and one that is better equipped to win new opportunities in an increasingly competitive global marketplace. Certifying your organization to ISO 9001, or other standards relating to quality, offers a proof of your commitment of business performance.
ISO 14001:2015
ISO 14001:EMS defines an effective environmental system which can be applied to all types of companies. Environmental issues have come to the forefront in recent years with greater awareness amongst legislators, insurers, financiers, shareholders, customers, employees and neighbors. It reduces the environmentally harmful effects of companies operations and by reducing the raw material and energy consumption it increases the financial efficiency of a company.

The system encourages the companies to use the environmental friendly, advanced production technologies.

ISO 14001:specifies the most important requirements to identify, control and monitor the environmental aspects of any organization, and also how to manage and improve the whole system.

ISO 14001:is part of a series of international standards applicable to any organization, anywhere, relating to environmental management. Based on the Plan-Do-Check-Act cycle, ISO 14001 specifies the most important requirements to identify, control and monitor the environmental aspects of any organization, and also how to manage and improve the whole system.
OHSAS 18001:2007
OHSAS 18001 Occupational Health & Safety Assessment Specification
Occupational Health and safety assessment Specification (OHSAS) is an international standard giving requirements related to health and safety management systems in order to enable an organization to control its risks and improve its performance.

OHSAS 18001: helps the organization to define the occupational health and safety policies and objectives including compliance to legal and other requirements. The organization can apply the standard to minimize risks, accidents and hazards, to improve employee motivation and involvement. Using professional assessment teams with in depth knowledge of your health & safety issues, the certification process will ensure that your management system meets the requirements of current Occupational Health & Safety Management Standards.
ISO IEC 27000
ISO 27001 Information security Management System

Information is an important asset & is valuable to an organization and hence needs to be suitably protected. Information leaks enhance risk. ISMS outlines the best practices that one should follow to protect informational assets ISMS the only method that specifically addresses the protection of information. It provides detailed guidelines on how a secure management framework should be implemented. Recent high profile information security breaches and the value of information are highlighting the ever increasing need for organizations to protect their information. An Information Security Management Systems (ISMS) is a systematic approach to managing sensitive company information so that it remains secure. It encompasses people, processes and IT systems..
ISO 31000: 2009
ISO 31000: 2009 Risk Management

ISO 31000: 2009 Risk managementRisks affecting organizations can have consequences in terms of economic performance and professional reputation, as well as environmental, safety and societal outcomes. Therefore, managing risk effectively helps organizations to perform well in an environment full of uncertainty. ISO 31000:2009 provides principles and generic guidelines on risk management. ISO 31000 Risk management ISO 31000:2009 can be used by any public, private or community enterprise, association, group or individual. Therefore, ISO 31000:2009 is not specific to any industry or sector.
ISO 15189: 2012
ISO 15189: 2012 Medical Laboratories

ISO 15189: 2012 Medical Laboratoriesis the international standard recognized for medical device regulations around the world.

ISO 15189 Medical laboratories - Particular requirements for quality and competence specifies the quality management system requirements particular to medical laboratories. The standard was developed by the International Organization for Standardizations’ Technical Committee 212 (ISO/TC 212). ISO/TC 212 assigned ISO 15189 to a working group to prepare the standard based on the details of ISO/IEC 17025:1999 General requirements for the competence of testing and calibration laboratories. This working group included provision of advice to users of the laboratory service, the collection of patient samples, the interpretation of test results, acceptable turnaround times, how testing is to be provided in a medical emergency and the lab's role in the education and training of health care staff.

ISO 15189: 2012 Medical Laboratoriesis the latest version of ISO 15189:2012, published in July 2003. This standard is based on the ISO 9001:2000 process model approach. All requirements of ISO 13485 are specific to organisations providing medical devices, regardless of the type or size of the organisation.
ISO 22000
ISO 22000 Food Safety Systems ISO 22000 Food safety is a global concern. Public health issues can significantly impact on trade. Legislation, in most countries, requires proprietors of food companies to implement HACCP principles into food production systems. A management system based on HACCP principles allows organizations to identify, document, maintain and review food hazards that occur during the food production process.

The International Organization for Standardization (ISO) 22000:2005 Standard: Requirements for a Food Safety Management System demonstrates an organization’s commitment to food safety, and provides a means to demonstrate that an organization is taking the necessary steps to control food safety hazards.
ISO 13485
ISO 13485 Certification ISO 13485is the international standard recognized for medical device regulations around the world. It is intended to promote harmonisation in the medical device industry and set a basis for quality system regulations worldwide. We provide services that help manufacturers understand what they need to do to place compliant devices on markets throughout the world.
ISO 13485: 2003:is the latest version of ISO 13485, published in July 2003. This standard is based on the ISO 9001:2000 process model approach. All requirements of ISO 13485 are specific to organisations providing medical devices, regardless of the type or size of the organisation.
ISO 30000
ISO 30000 Ships and Marine Technology

ISO 30000 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.
ISO 17025:2005
ISO/IEC 17025:2005 General requirements for the competence of testing and calibration laboratories. > ISO/IEC 17025:2005 specifies the general requirements for the competence to carry out tests and/or 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 and/or calibrations. These include, for example, first-, second- and third-party laboratories, and laboratories where testing and/or calibration forms part of inspection and product certification. ISO/IEC 17025:2005 is applicable to all laboratories regardless of the number of personnel or the extent of the scope of testing and/or calibration activities. When a laboratory does not undertake one or more of the activities covered by ISO/IEC 17025:2005, such as sampling and the design/development of new methods, the requirements of those clauses do not apply. ISO/IEC 17025:2005 is for use by laboratories in developing their management system for quality, administrative and technical operations. Laboratory customers, regulatory authorities and accreditation bodies may also use it in confirming or recognizing the competence of laboratories. ISO/IEC 17025:2005 is not intended to be used as the basis for certification of laboratories. Compliance with regulatory and safety requirements on the operation of laboratories is not covered by ISO/IEC 17025:2005.
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