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Benefits of ISO 22000:2005 Certification Implementing ISO 22000 will bring the following benefits to your organization : An auditable standard with clear requirements which provides a framework for third-party certification Suitable for regulators The structure aligns with the management system clauses of ISO 9001 and ISO 14001 Enables communication about hazards with partners in the supply chain System approach, rather than product approach Applicable to all organizations in the global food supply chain Systematic management of prerequisite programmes Increased due diligence Dynamic communication on food safety issues with suppliers, customers, regulators and other interested parties signifies that it is a truly global international standard Provides potential for harmonization of national standards Covers the majority of the requirements of the current retailer food safety standards Complies with the Codex HACCP principles Provides communication of HACCP concepts internationally A systematic and proactive approach to identification of food safety hazards and development and implementation of control measures Resource optimization internally and along the food chain All control measures are subjected to hazard analysis Better planning-less post process verification Improved documentation.

The ISO13485 is a quality system standard for organizations that design, develop, produce or service medical devices. It is intended to promote harmonization in the medical device industry and set a basis for quality system regulations worldwide. All requirements of ISO13485 are specific to organizations providing medical devices, regardless of the type or size of the organization. The certification of a quality management system, specifically for medical devices to ISO13485 proves advantageous, and in many cases essential, for medical companies which export their products to global markets. Some of the additional requirements relate to design controls, process controls (including environmental controls), special processes, traceability, record retention, and regulatory actions, which are more critical for the medical device industry. An ISO13485 compliant management system adopt a risk management approach which includes assessment to identify & estimate risk, uses risk controls and techniques with a view to eliminate hazardous situations throughout product realization. Adopting this standard is beneficial to the organization in many ways : It demonstrates the manufacturer's ability to supply medical devices and related services that are compliant with all regulatory requirements.Assures the customers that the product complies with all relevant product and service-oriented technical standards and regulations.Emphasizes the cleanliness and sterility in the production area, which in turn increases efficiency and enhances safety at the workplace.Organization establishes for risk management throughout the product realization.

“empowering india-powering the world” enable the poor and marginalized to access benefits. Greater assistance for placing candidates. Switch in focus from training to career progression. Inclusive program design. Iso is an autonomous international organization that promotes invention and conducts way to the advancement of trade. The purpose of getting yourself iso registered is to promote the advancement of standardization in technology. Iso has listed internationally acknowledged standards (e.g., 9001, 22000, 14000) to promote worldwide exchange of goods. Iso registration or iso certification enhances the reliability of your business and assists you get more business. You might have seen iso 9001 quality mark on commodities from large companies. This can be achieved through iso certification. Companies desiring to achieve iso certifications, iso registration process or iso certificates comprising iso 9001, iso 14001, iso 20000, ohsas 18001, iso 50001, iso 27001, iso ts 16949 etc. Certification in india can contact skill development advisor. Documents required for iso registration copy of pan card copy of aadhaar card/ voter identity card passport size photograph. two copies of sales bill/purchase bill

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ISO 50001:2011, Energy management systems – Requirements with guidance for use, is a voluntary International Standard developed by ISO (International Organization for Standardization). ISO 50001 gives organizations the requirements for energy management systems (EnMS). ISO 50001 provides benefits for organizations large and small, in both public and private sectors, in manufacturing and services, in all regions of the world. ISO 50001 will establish a framework for industrial plants, commercial, institutional, and governmental facilities and entire organizations to manage energy. Targeting broad applicability across national economic sectors, it is estimated that the standard could influence up to 60 % of the world's energy use.

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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 162 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. We provide Consultancy, Inspection, Internal Audit Tearing, Certification and Renewal of the followings ISO Standards ISO 9001: 2008 Certification ISO 9000 stands for International Organization of Standardization, created in 1947. It is a worldwide federation of �Member Bodies� (i.e., National bodies � Government Institution or Organization incorporated by Public Law) with it's headquarter at Geneva, Switzerland. India is represented by BIS (Bureau of Indian Standards). ISO 9001:2008 specifies requirements for a quality management system where an organization : Needs to demonstrate its ability to consistently provide product that meets customer and applicable statutory and regulatory requirements.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 customer and applicable statutory and regulatory requirements. ISO is important because of its systemic orientation. We think this is crucial. Many people in this field wrongly emphasize motivational and attitudinal factors. The assumption is that quality can only be created if workers are motivated and have the right attitude. This is fine, but it doesn't go far enough. Unless you institutionalize the right attitude by supporting it with the right policies, procedures, records, technologies, resources, and structures, you will never achieve the standards of quality that other organizations seem to be able to achieve. Unless you establish a quality attitude by creating a quality system, you will never achieve a world-class standard of quality. Advantages of ISO 9001:2008 Passport for Global marketReflect ProfessionalismCreate credibility among new business segment.Improved quality, reduction in costClarity of responsibility and authorityBetter and defined systemConsistent quality and performanceImproved Cycle TimeStructured work culture to drive the process of businessReduction of variation and waste in supply chainCustomer satisfaction through regular interaction ISO 14001 : 2004 Certification The ISO 14001 standards are designed to provide an internationally recognized framework for environmental management, measurement, evaluation and auditing. A system compliant to ISO14001 is a management system dedicated to manage the environmental issues of an organization. A Certified Environmental Management System proves that the business is taking active steps to fulfill social & environmental responsibilities. Environmentally credible companies have a competitive edge in national and international markets. An �Environmental Management System� helps the organization to be in control of and successfully manage the most significant environmental aspects, e.g. emissions, waste-handling, utilize natural resources and energy-efficiency together with compliance to environmental regulations. ISO 13485: 2003 Certification The ISO13485 is a quality system standard for organizations that design, develop, produce or service medical devices. It is intended to promote harmonization in the medical device industry and set a basis for quality system regulations worldwide. All requirements of ISO13485 are specific to organizations providing medical devices, regardless of the type or size of the organization. The certification of a quality management system, specifically for medical devices to ISO13485 proves advantageous, and in many cases essential, for medical companies which export their products to global markets. Some of the additional requirements relate to design controls, process controls (including environmental controls), special processes, traceability, record retention, and regulatory actions, which are more critical for the medical device industry. An ISO13485 compliant management system adopts a risk management approach which includes assessment to identify & estimate risk, uses risk controls and techniques with a view to eliminate hazardous situations throughout product realization. ISO / TS 16949: 2002 Certification The ISO/TS 16949:2002 standard is the consensus of international quality requirements, which consists of policies and procedures that ensures worldwide consistence with the suppliers of parts, materials, or finishing services. How do automotive manufacturers assure that the numerous parts that they receive from suppliers are of the highest quality?  How do automobile manufactures assure that suppliers provide products that manufacturers can be responsible for and are worthy of the manufacturers name?  Automotive manufacturers assure quality by requiring registration to automotive quality standards that provide quality assurance. ISO/TS 16949:2002 is the latest automotive quality standard which was developed to be a new universally accepted quality standard for automobile suppliers. The ISO/TS 16949:2002 standard was developed to be an automotive standard for the customers� of automotive manufacturers and it is aligned with the ISO-9001: 2002 standard. The purpose of ISO/TS 16949:2002 was to create standardization in the quality management standards for automobile suppliers throughout the world. ISO/TS 16949:2002 is a process approach quality standard, which places requirements that assure consistent quality, throughout organizations that supply automobile manufacturers. By requiring ISO/TS 16949:2002 certifications, automobile manufacturers can be assured that all of their suppliers are adhering to a consistent set of quality standards that are strict and intertwined throughout the supplier�s organization. OHSAS 18001: 2007 Certification The Occupational Health and Safety Assessment Series (OHSAS) specification 18001 and the accompanying guideline OHSAS 18002 have been developed in response to urgent customer demand for a recognizable occupational health and safety management system standard against which their management systems can be assessed and certified. OHSAS 18001 is also compatible with the ISO 9001:2008 quality management system and ISO 14001:2004 environmental management system standards, in order to facilitate the integration of quality, environmental and occupational health and safety management systems by organization, if they wish to do so. The specification takes a structured approach to OH&S management. The emphasis is placed on practices being pro-active and preventive by the identification of hazards and the evaluation and control of work related risks. OHSAS 18001 can be used by organization of all sizes regardless of the nature of their activities or location. Organizations can now achieve third party certification for their Occupational Health and Safety management system. ISO 22000 : 2005 / HACCP Certification 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 consumerTo demonstrate compliance with applicable statutory and regulatory food safety requirementsTo evaluate and assess customer requirements and demonstrate conformity with those mutually agreed customer requirements that relate to food safety, in order to enhance customer satisfactionTo effectively communicate food safety issues to their suppliers, customers and relevant interested parties in the food chainTo ensure that the organization conforms to its stated food safety policyTo demonstrate such conformity to relevant interested partiesTo 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. ISO 27000: 2005 Certification An Information Security Management System (ISMS) provides a systematic approach to managing sensitive information in order to protect it. It encompasses employees, processes and information systems. The world renowned British Standard for Information Security Management Systems, BS 7799-2:2002, has been updated and was released on the 15 October 2005 as an international standard, ISO/IEC 27001:2005. ISO 27001 defines comprehensive requirements for ISMS that deals with all the technical and Human aspects in information security in all its operational processes. Companies can be independently audited to ISO 27001and achieve registration to show their customers, partners and regulatory bodies that their processes are secured in handling information. SO 27001 refer to ISO 17799 for implementation guidance and include an abstract of ISO 17799 as an appendix showing auditors the kinds of control to expect. The goal of ISO 27001 is to provide a common base for developing organizational security standards and effective security management practice and to provide confidence in inter-organizational dealings. SA 8000 Certification SA 8000, or "Social Accountability 8000", was developed to promote socially responsible business in all sectors around the globe. Rather than being a "sweatshop code" for customers to enforce upon their suppliers, SA8000 was developed to help socially responsible companies to measure and differentiate themselves from other companies operating with less than acceptable labor conditions. It sets out expectations regarding health and safety, child labor, forced labor, freedom of association, discrimination, disciplinary practices, working hours and compensation together with the management systems to deliver them. SA8000 covers all the major labor rights issues contained in International Labor Organization (ILO) conventions, the Universal Declaration of Human Rights and the UN Convention on the Rights. CE Marking What does CE marking mean? What do the initials CE stand for? CE marking is a declaration by the manufacturer that the product meets all the appropriate provisions of the relevant legislation implementing certain "European Directives". "CE marking" gives companies easier access into the European market to sell their products without adaptation or rechecking. The initials "CE" do not stand for any specific words but are a declaration by the manufacturer that his product meets the requirements of the applicable European Directives. The actual CE Marking is the letters "CE" which a manufacturer affixes to certain products for access to the European market (consisting of 18 countries and also referred to as the European Economic Area or EEA). The letters "CE' are an abbreviation of a French phrase "Conformity European". The marking indicates that the manufacturer has conformed with all the obligations required by the legislation. Initially, the phrase was "CE Mark": however, "CE Marking" was legislated as its replacement in 1993.  "Manufacturers are responsible for ensuring that the products they place on the market meet all relevant regulations. Where these regulations do not require mandatory certification, manufacturers often seek voluntary certification to assure themselves that their products do meet the requirements set by law." Please Note The CE Marking is not a quality-mark. First, it refers to the safety rather than to the quality of a product. Second, CE marking is mandatory for the product it applies to whereas most quality marking are voluntary.Many people use the term �CE Mark�. Initially, this was the phrase used to indicate this conformity marking. However, �CE mark� was officially replaced by the term �CE Marking� in 1993. Thus, it is better to speak of �CE Marking�. The main goals of the CE Marking are to : indicate a product's conformity with the "essential requirements" of the directivesAllow products to be "placed on the market"Ensure the "free movement of goods"Allow the "withdrawal of non-conforming products" by customs and enforcement authorities The CE Marking is not a mark or certification or approval issued by a third partyis not simply a marketing or promotional toolis not a quality markis not for components* Although there are some exceptions, the vast majority of components do not need CE Marking.

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We provide ISO Certification services to our valued clients which covers different type of ISO Certificates. We provide services for the certification for ISO9001:2008, ISO-22000, ISO14001:2004 and OHSAS-18001. ISO9001:2008 is an international standard that can be applied to any size of the organization for both services and products. The standard consists of a set of requirements that specify that what an organization must do. The ISO 9001 is a Quality Management Certification System, which enables you to show your commitments towards quality and customer satisfaction. ISO14001:2004 is an environment management system. It provides guidance on how to manage the environment aspects of business activities in efficient way while taking into account the pollution control. It is a tool that can be used for following purposes. Providing assurance on environment issues to customers and societyProviding assurance to management of clean environmentAssuring employees that they are working in pollution free environment ISO-22000: Food Safety Management System An international standard defines the requirements of a food safety covering all organizations in the food chain including catering and packing companies. OHSAS-18001 It enables an organization to manage operational risks and improve performance. It provides guidance on how to manage the health and safety aspects of all the business activities in more efficient way considering accidents preventions, risk reduction etc.

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