What is ISO 9001 QMS?ISO 9001 Quality Management System provides the basic standard guidance and tools for companies and organizations to ensure that the quality of products and services are consistently metAs the world’s most widely recognized Quality Management Standard, ISO 9001 outlines the ways to achieve, as well as benchmark, consistent performance and service. It covers the basic concepts and sets out requirements on how to have a World Class Quality Management Systems which allows you to become a more consistent competitor in your marketplace. ISO 9001 quality management system will help you to continually monitor and manage quality across all operations as it aims to enhance customer satisfaction through the effective application of the system, including processes for continual improvement of the system and the assurance of conformity to customers and applicable statutory and regulatory requirements. ISO 9001 is suitable for organisations in all industry sectors and will help your organisation to improve management processes to compete locally and/or globally. |
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What is ISO 14001 EMS?ISO 14001 Environment Management System designed for companies that are looking to manage its environmental responsibilities in a strategic manner that contributes to the world's sustainability effortISO 14001 is an internationally accepted standard that outlines how to put an effective environmental management system in place. Customers, consumers, and shareholders are increasingly concerned on the environmental impacts of their products, activities and services they consume or provide to the society. ISO 14001 is designed to help businesses remain commercially successful without overlooking environmental responsibilities. It can also help you to grow while reducing the environmental impact and stand out from competition as a proof of your commitment towards protecting the environment. An ISO 14001 system provides the framework to allow you to meet increasingly high customer expectations of corporate responsibility as well as legal or regulatory requirements. |
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What is AS/EN 9100 AMS ?AS/EN 9100 Aerospace Management System designed specifically for the aerospace industry to ensure the highest quality standards are met globally in all parts of the supply chainAS 9100 is the US version of a globally harmonised quality management system standard developed by the International Aerospace Quality Group for aerospace industries. AS 9100 is based on the international Quality Management System (QMS) standard, ISO 9001 with additions and interpretations specifically caters for the aviation space and defence industry sectors. It supplements ISO 9001 by focusing on the unique, complex, and highly regulated nature of the aerospace industry. Specifically, it emphasises the critical aspects of key characteristics and the need to satisfy internal, governmental and regulatory requirements. AS 9100 has some associated standards, including 9110 which is designed for repair and overhaul organisations and 9120 which is designed for distributor stockholders. The International Aerospace Quality Group (IAQG) publishes these standards. Type of Certification
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What is ISO 45001 OH&S ?ISO 45001 Occupational Health and Safety help companies to improve employee safety, reduce workplace risks and create a better and safer working conditionISO 45001 is a framework for an occupational health and safety management system. It can help you put in place the policies, procedures and controls needed for your organization to achieve the best possible working conditions, aligned to internationally recognized best practice. An organization’s OH&S management system can translate its intentions to prevent incidents into a systematic and ongoing set of processes (supported by the use of appropriate methods and tools) and can reinforce the organization’s commitment to proactively improving its OH&S performance. OHSAS 18001 Management System takes into account the organisational structure, planning activities, responsibilities, practices, processes and resources for developing, implementing, achieving, reviewing and maintaining the organisation’s OH&S policy. |
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What is IATF 16949?IATF 16949 Automotive Management System provide companies standards for continual improvement, defect prevention and the reduction of variation and waste in the supply chainIATF 16949 is the global technical specification and quality management standard for the automotive industry. It provides continual improvement, emphasising on defect prevention and the reduction of variation and waste in the automotive supply chain. IATF 16949 outlines everything you need to know about achieving best practice when designing, developing, manufacturing, installing or servicing automotive products. IATF 16949 was written by the International Automotive Task Force (IATF) that consisted of participating members like BMW, DaimlerChrysler, Fiat, Ford Motor Company, General Motors (including Opel Vauxhall), PSA Peugeot – Citroen, Renault SA, Volkswagen and trade associations such as AIAG (US), ANFIA (Italy), FIEV (France), SMMT (UK) and VDA (Germany). |
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What is ISO 50001 EnMS ?ISO 50001 Energy Management Systems is designed to enable an organisation to follow a more systematic and practical approach to improve energy performance such as Energy use, Energy efficiency, Energy consumption is all sectors of the organisation.This energy Management System helps organisation continuously improve on energy use which therefore reducing energy cost, greenhouse emissions, etc. This system is build based on the ISO 9001 QMS, ISO 14001 EMS which consist of clauses modular with both. This also makes organisation to implement ISO 50001 EnMS easier when integrating energy management into their overall efforts of Quality and environmental management. |
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What is ISO 13485 MED?ISO 13485 MED specifies the requirements for a quality management system for companies providing medical devices and related services that meets regulatory standardsISO 13485:2003 specifies the requirements for a quality management system for organizations who provide medical devices and related services to consistently meet customer requirements and regulatory requirements in the medical industry. Adopting ISO 13485 provides a practical foundation for manufacturer to address the medical device directives, responsibilities, regulations as well as demonstrating a commitment to provide reliable quality and safety of medical devices. |
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What is ISO 22000?ISO 22000 designed to help companies meet ISO’s food safety management standards and help companies identify and control food safety hazards across the world.ISO 22000 family of International Standards addresses Food Safety Management. It defines the requirements on how to manage food safety covering all organizations in the food chain from “Farm to Fork”. The consequences of unsafe food can be serious and ISO’s food safety management standards help organizations to identify and control food safety hazards. As many of today’s food products repeatedly cross national boundaries, International Standards are needed to ensure the safety of the global food supply chain. ISO 22000 is also for companies seeking to integrate their quality management system, for example ISO 9001, and their food safety management system.The standard combines generally recognised key elements to ensure food safety along the food chain including the control of food safety hazards with Hazard Analysis & Critical Control Points (HACCP). |
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What is ISO 17025 LAB?ISO 17025 LAB enables laboratories around the world to demonstrate the standards required to operate competently, consistently and generate valid resultsISO 17025 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. This standard sets out valid specifications to improve organization’s quality assurance systems and quality control and ensure organisation are technically competent and can generate technically valid results. ISO 17025 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. |
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What is ISO 37001 ABMS?ISO 37001 Anti-Bribery Management system is designed to tackle all sorts of bribery, fraud and unethical or suspicious actions in an organisation with a management system recognised internationally.This Anti-Bribery Management System aims to help organisation to prevent, detect and respond to any bribery incidences that occurred in the past, present or the future. This standard also complies with laws, regulations and other voluntary commitments. Bribery risk is one of the significant risk that are faced by organisations of all sizes, sectors and nature of business. Addressing and confronting bribery requires an organisation to follow strict SOPs such as adopting an anti-bribery policy, appointing an overseer on anti-bribery compliance, due diligence on business operations and associates. |
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