Minimum Order Quantity | 5 Certificate |
Service Location | Pan India |
Payment Mode | Online |
Duration | Same Day |
Service Type | Greenguard Certification Service |
Service Mode | Online |
Brief explanation of Green Guard Certification
Green Certification is a rigorous program that products for low chemical emissions. This program is designed to ensure that products do not cause indoor air pollution and contribute to harmful effects on human health. The certification is conducted by the Greenguard Environmental Institute, which is a non-profit organization recognized globally. The program has two tiers of certification: Green Guard and Green Guard Gold. The latter has even higher standards of testing and is recommended for those who are more sensitive to air pollution, such as children or elderly people. The certification process involves testing products in specially-designed testing chambers for up to two weeks, where they are subjected to controlled temperatures and humidity levels. The testing checks for over 10,000 chemicals and VOC emissions, ensuring that the products meet the strict standards of low emission levels set by the certification program. Obtaining Green Guard Certification shows a manufacturer’s commitment to a healthier environment and can provide a competitive advantage by appealing to consumers who are more health- and environment-conscious.
Significance of the certification in India
Green Guard Certification is becoming increasingly significant in India due to the rapid industrialization and urbanization in the country. The certification ensures that the products or materials used inside buildings have low chemical emissions, which improves the indoor air quality and reduces exposure to harmful chemicals. The certification is especially important for schools, healthcare facilities, and homes, where people spend most of their time indoors. With the rising concern over indoor air pollution and its impact on human health, the certification has become a benchmark of quality for manufacturers in India. Green Guard certification gives Indian manufacturers a competitive edge by enhancing their reputation and promoting their commitment to protecting human health and the environment. Moreover, with the stringent regulations and standards put in place by the government, the certification has become a necessity for manufacturers to ensure that their products comply with the required standards and regulations. In conclusion, Green Guard certification is an important tool for promoting healthier indoor environments in India and building a sustainable future.
The purpose of Green Guard Certification
The purpose of Green Guard Certification is to ensure that products and materials have low chemical emissions that are safe for human health. With the growing concern of indoor air pollution and its impact on human health, Green Guard Certification provides a solution to help improve indoor air quality. By testing products in strict testing chambers, the certification ensures that they emit minimal volatile organic compounds (VOCs) which are harmful chemicals that can lead to respiratory diseases and cancer. Green Guard Certified products also provide manufacturers with a competitive advantage, as they demonstrate their commitment to sustainability and health.
Service Location | Pan India |
Service Type | IEC 61010-1:2010 Safety Requirement Certification Service |
Duration | 10 Days |
Service Mode | Online |
Payment Mode | Online |
IEC 61010 provides safety guidelines and requirements for electrical equipment used in various settings, including laboratories, measurement and control systems, and similar environments. Its primary objective is to ensure the safety of personnel who work with or are in proximity to such equipment.
The standard covers a wide range of electrical equipment, including but not limited to:
IEC 61010 specifies safety features, protective measures, and performance requirements for these types of equipment as well as addresses various potential hazards, such as electrical shock, fire, mechanical hazards, and hazards related to energy sources.
Benefits of IEC 61010Compliance with IEC 61010 is essential for manufacturers, designers, and users of electrical equipment, as it helps ensure the safety of both operators and the surrounding environment. The standard is regularly updated and revised to keep pace with technological advancements and evolving safety practices.
IEC 61010 also helps identify and mitigate potential risks associated with electrical equipment. The standard addresses a wide range of hazards, including electrical, mechanical, and energy-related risks. By incorporating safety features and protective measures outlined in the standard, the likelihood of accidents, injuries, and property damage can be significantly reduced.
Minimum Order Quantity | 5 Certificate |
Service Location | Pan India |
Service Mode | Online |
Payment Mode | Online |
Duration | Same Day |
Service Type | Halal Certification Services |
Halal Certification is predominantly obtained for food and food-related products, and it is essential in Islamic countries. The term "Halal" is derived from the Quran, which means "permitted" or "lawful." Therefore, according to Islamic law, the Shariah, the Certification is used for Food and other consumables permissible for consumption. Halal Certification emphasizes cleanliness in all aspects of a person's life, and Halal foods ensure that the Food consumed by individuals is clean, hygienic, and does not harm their health or well-being. The Certification guarantees that the food product is safe for consumption. With the increasing awareness of Halal foods, more businesses are seeking Halal Certification for their products, restaurants, premises, etc.
Halal Certification in IndiaIn India, a Halal Certificate is a document issued by a Halal certification body or authority confirming that a product or service complies with Islamic dietary laws and guidelines and is permissible or "Halal" for consumption by Muslims.
Halal Certification in India is significant for food and beverage products, pharmaceuticals, and personal care products. Still, it can also apply to other non-food products or services. Businesses seeking Halal Certification in India must comply with the relevant standards and guidelines set forth by the certification body or authority and undergo a rigorous inspection and audit process to ensure compliance.
Types of Halal CertificationThe type of Halal Certification varies depending on the nature of the business. Typically, restaurants, hotels, slaughterhouses, and packaging and labeling materials seek Halal Certification to ensure they meet the requirements of Muslim consumers. However, Halal Certification is not limited to food production alone. Other products, such as non-alcoholic beverages, raw materials for food processing, pharmaceutical and healthcare products, traditional herbal products, cosmetics, personal care products, cleaning products, and everyday consumer goods, can also obtain Halal Certification.
Halal Certification Bodies offer Certification under various schemes, including the Food, and Catering Scheme, Restaurant Scheme, Industrial Scheme, Abattoir Scheme, Warehouse or Storage Scheme, and Product Endorsement Scheme.
Advantages of expanding your business, the Halal wayThe benefits of obtaining a Halal Certificate in India are numerous. Here are some of the key benefits:
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Minimum Order Quantity | 5 Certificate |
Service Mode | Online |
Payment Mode | Online |
Duration | Same Day |
Service Type | ROHS Certification Service |
Service Location | Pan India |
RoHS
RoHS stands for Restriction of Hazardous Substances, which is also known as the Directive 2002/95/EC. It includes the restrictions for the use of certain hazardous substances in electrical and electronic equipment. RoHS is a WEEE (Waste of Electrical and Electronic Equipment). The European Directive on the Restriction of Hazardous Substances (RoHS) holds electrical and electronic equipment companies directly responsible for the chemical compliance of their products. This means all products must conform to strict standards, provide extensive compliance documentation, and ensure that electrical and electronic products sold in the EU do not contain lead, cadmium, mercury, hexavalent chromium, polybrominated biphenyls (PBBs), and polybrominated diphenyl ethers (PBDEs) above the legal threshold. Manufacturers, owners, retailers, and importers alike need to ensure that their products comply in order to be distributed and sold in the EU.
In India, demand for electronic products is increasing widely, due to which the environment and human health are in danger. Furthermore, rapidly evolving technologies encourage consumers to discard electronic devices quickly, resulting in an alarming increase in the amount of electronic trash. Keeping this in consideration all the harmful effects of electronic waste, The Ministry of Environment and Forest (MoEF) and the Government of India implemented the Restriction of Hazardous Substance, which in India is known as Electronic waste.
Depending on the size of the Indian legal entity and the type of imported devices, you may be subject to WEEE or RoHS responsibilities if you produce or import electronic products in the Republic of India.
SUBSTANCES PROHIBITED UNDER ROHS CERTIFICATIONIntertek does more than simply help our customers comply, we give them a competitive advantage by partnering with them every step of the way to establish a detailed product file upon application that contains:
All compliance documents are subject to review and samples are required for RoHS 6-substance verification and testing of homogeneous materials. In addition, manufacturer site audits and surveillance for process management control will be implemented and executed to ensure compliance.
This unique Intertek certification scheme essentially offers:
Minimum Order Quantity | 5 Certificate |
Service Type | ISO 14001:2015 Certification Service |
Payment Mode | Online |
Service Location | Pan India |
Service Mode | Online |
Duration | Same Day |
ISO 14001 is the internationally recognized standard for environmental management systems (EMS). It provides a framework for organizations to design, implement, and continually improve their environmental performance. By adhering to this standard, organizations can ensure they are taking proactive measures to minimize their environmental footprint, comply with relevant legal requirements, and achieve their environmental objectives. The framework encompasses various aspects, from resource usage and waste management to monitoring environmental performance and involving stakeholders in environmental commitments.
Why is ISO 14001 important?In an age of heightened environmental consciousness and increasing global challenges such as climate change, biodiversity loss, and resource depletion, organizations have a pivotal role to play. ISO 14001 offers a structured approach for businesses to address these pressing concerns. By adopting this standard, organizations signal a commitment not only to regulatory compliance but also to ongoing environmental improvement. This proactive approach to environmental management can result in tangible benefits, such as reduced waste, energy conservation, and cost savings.
Furthermore, it enhances an organization's reputation, fosters stakeholder trust, and often meets a critical criterion for engaging in global trade and supply chains. Simply put, ISO 14001 stands as a testament to an organization's dedication to a sustainable future, blending environmental responsibility with strategic business growth.
Minimum Order Quantity | 5 Certificate |
Service Location | Pan India |
Payment Mode | Online |
Service Mode | Online |
Duration | Same Day |
Product/Service Code | 10001AQSPL |
Manage customer complaints effectively and you’ll have more chance of meeting their expectations as well. And you can quickly turn customer complaints into customer satisfaction instead – especially when you view complaints as an opportunity to improve what you do and how you do it. ISO 10002 can help you to achieve this whatever the size or nature of your business. The customer complaints management system is a basic but essential requirement for any business – especially businesses that want to become and remain successful.
What is ISO 10002 Customer Satisfaction. Complaints Handling?Customers expect more and more from the service you provide. And your competitors are working harder to meet these expectations. You can too with ISO 10002, the international standard for customer satisfaction. It provides you with guidelines for putting in place your own complaints management system – helping you to identify complaints, their cause and how to eliminate them. ISO 10002 will also allow you to identify areas in your business where you can improve and eventually remove the cause of complaints. The standard outlines management controls and processes that help you to handle customer complaints more effectively and efficiently – making sure that more customers are satisfied with the service you provide.
What are the benefits of customer complaint management?There are many reasons to work with us to introduce and implement customer complaints management. That’s because we established the first complaints management system standard in 1999 (BS 860). This provided the foundations for the international standard ISO 10002. We can use this experience and knowledge to help you become an expert in managing customer complaints with your own ISO 10002 management system.
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Minimum Order Quantity | 5 Certificate |
Service Location | Pan India |
Service Mode | Online |
Payment Mode | Online |
Duration | Same Day |
Service Type | ISO 14855-1:2012 Certification Consultancy Service |
Minimum Order Quantity | 5 Certificate |
Service Location | Pan India |
Service Type | ISO 3834-1:2021 Certification Service |
Service Mode | Online |
Payment Mode | Online |
Duration | Same Day |
SO 3834-1:2005 provides criteria to be taken into account for the selection of the appropriate level of quality requirements for fusion welding of metallic materials, among the three levels specified in ISO 3834-2:2005 ISO 3834-3:2005 and ISO 3834-4:2005. It applies to manufacturing, both in workshops and at field installation sites.
ISO 3834-1:2005 does not specify requirements for a total quality management system. However, quality management system elements where their inclusion will complement ISO 3834 are defined.
The Quality Management System is subject to EN ISO 3834-2,3,4. DIN/ČSN EN 15085 for the certification levels CL 1 to CL 4 currently applies to the competence of manufacturers in welding of railway vehicles and components. This applies for welding both in the workshop and on site. In relation to the specific Product Code, it determines the quality requirements of the welding work at three levels – higher – grade 2, medium – grade 3 and basic – grade 4. The required certification level is linked to specific applications and the relevant Product Code.
If the company has a certified quality system according to EN ISO 9001:2008 requirements, the certification level of the welding quality system according to EN ISO 3834-2 is also required. The quality system according to this standard is compatible with ISO 9001.
Certification of the manufacturers and assembly organizations (both in the workshop and on site) according to EN ISO 3834-2, 3, 4 – Quality requirements for fusion welding of metallic products. The standard consists of 6 parts:
Part 1: Criteria to be taken into account for the selection of the appropriate level of quality requirements are
Part 2: Comprehensive quality requirements
Part 3: Standard quality requirements
Part 4: Production requirements
Part 5: The documents with which it is necessary to conform to claim to the quality requirements of EN ISO 3834-2,3,4
Part 6: Guidelines for implementing ISO 3834
Special Welding Process is widely used in many key and small engineering and construction companies as an integral part of the main implementation process, affecting in various degrees the production of the final product. It is also often used in the foundry by means of repair welding. After its professional application, the product can be considered conforming.
The application of welding methods can be found in conjunction with simple products, up to very complex units, according to various product standards and legislative regulations. Our company deals with conformity assessment mainly in the so-called regulatory area where the conformity of the product with precisely defined Product Codes and legislative definitions for a given area is demonstrated. These are mainly links to the following areas of industry:
• pressure vessels
• pressure equipment
• boiler bodies
• nuclear facilities
• steel structures
• steel bridge structures
• aluminium structures
• railway vehicles, etc.
Minimum Order Quantity | 5 Certificate |
Service Location | Pan India |
Service Mode | Online |
Payment Mode | Online |
Duration | Same Day |
Service Type | ISO 9001:2015 Certification Service |
ISO 9001:2015
ISO 9001 is a globally recognized standard for quality management. It helps organizations of all sizes and sectors to improve their performance, meet customer expectations and demonstrate their commitment to quality. Its requirements define how to establish, implement, maintain, and continually improve a quality management system (QMS).
Implementing ISO 9001 means your organization has put in place effective processes and trained staff to deliver flawless products or services time after time.
Why is ISO 9001 important?With more than one million certificates issued to organizations in 189 countries, ISO 9001 is the most widely used quality management standard in the world. Within the ISO 9000 family, which defines seven quality management principles including a strong customer focus and continual improvement, ISO 9001 is the only standard that can be certified to (though certification is not mandatory).
Business benefits include:
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Minimum Order Quantity | 5 Certificate |
Service Location | Pan India |
Service Mode | Online |
Payment Mode | Online |
Duration | Same Day |
Service Type | ISO IEC 27001:2022 Certification Service |
ISO/IEC 27001 is the world's best-known standard for information security management systems (ISMS). It defines requirements an ISMS must meet.
The ISO/IEC 27001 standard provides companies of any size and from all sectors of activity with guidance for establishing, implementing, maintaining and continually improving an information security management system.
Conformity with ISO/IEC 27001 means that an organization or business has put in place a system to manage risks related to the security of data owned or handled by the company, and that this system respects all the best practices and principles enshrined in this International Standard.
Why is ISO/IEC 27001 important?With cyber-crime on the rise and new threats constantly emerging, it can seem difficult or even impossible to manage cyber-risks. ISO/IEC 27001 helps organizations become risk-aware and proactively identify and address weaknesses.
ISO/IEC 27001 promotes a holistic approach to information security: vetting people, policies and technology. An information security management system implemented according to this standard is a tool for risk management, cyber-resilience and operational excellence.
BenefitsAn information security management system that meets the requirements of ISO/IEC 27001 preserves the confidentiality, integrity and availability of information by applying a risk management process and gives confidence to interested parties that risks are adequately managed.
Minimum Order Quantity | 5 Certificate |
Service Location | Pan India |
Service Mode | Online |
Payment Mode | Online |
Duration | Same Day |
Service Type | ISO 13485:2016 Certification Service |
ISO 13485 is a crucial international standard designed to enhance the quality management systems of organizations involved in manufacturing medical devices and equipment. This certification outlines stringent control measures to minimize operational errors in the manufacturing process and emphasizes continual improvement in the quality of medical equipment.
Defining Medical DevicesA medical device encompasses instruments, machines, implants, or in vitro reagents used for diagnosing, preventing, or curing diseases or medical conditions. This broad category includes diverse items such as:
ISO 13485 certification is imperative for organizations engaged in designing and manufacturing medical devices and equipment. This certification establishes and maintains a quality management system, ensuring the safety of professionals and patients in clinics, hospitals, and other medical facilities.
ISO 13485 Certification for BusinessesOrganizations involved in the design, production, installation, and servicing of medical devices and related services can benefit from ISO 13485 certification. Regulatory authorities and certifying organizations utilize ISO 13485 certification as a baseline for quality assurance during compliance evaluations. This recognition positions certified organizations as reputable and trustworthy providers adhering to international standards of quality and safety.
ISO 13485 Certification RequirementsTo achieve ISO 13485 certification, organizations must meet specific standards outlined in the ISO 13485 requirements. These include a review of design controls, development and management of ISO-compliance documentation, quality risk analysis, peer review as evidence of ISO compliance, identification of ISO-mandated documents, an ISO training plan, and internal ISO audits. Adhering to these requirements ensures that organizations meet minimum patient safety, healthcare quality, and regulatory standards.
The ISO 13485 Certification Process
Embarking on the ISO 13485 certification journey involves a structured process designed to assess and validate an organization’s commitment to quality management in medical device manufacturing. The ISO 13485 certification process encompasses several key stages, each integral to achieving certification and demonstrating compliance with ISO 13485 standards.
The journey begins with the submission of an application for ISO 13485 certification. This initial step involves a comprehensive review of the organization’s details, scope of operations, and specific requirements. A contractual agreement is established, outlining the terms and conditions for the ISO 13485 certification process
Minimum Order Quantity | 5 Certificate |
Service Location | Pan India |
Payment Mode | Online |
Duration | Same Day |
Service Type | ISO 21001:2018 Certification Service |
Service Mode | Online |
ISO 21001 Certification for Educational Organization Management System (EOMS) provides a framework for establishing flexible, transparent and inclusive classrooms and enables an organization to provide personalized learning to meet the needs and requirements of the individual learner. It helps educational organizations to implement the best practices and aims to improve the quality of education by providing the necessary training to the teachers.
ISO 21001 certification promotes a learner-centric approach and actively engages learners in their own learning. It was published in 2018 by the International Organization for Standardization (ISO) to allow educational institutions to provide high-quality services. It promotes equitable and accessible education for all and offers more personalized learning for learners with special needs and distance learners.
Any educational organization can apply for ISO 21001 certification, including private and private, regardless of size, nature and location. A list of organizations that can go for ISO 21001 certification for Educational Organization Management System (EOMS) is as follows:
The Educational Organization Management System (EOMS) is not restricted to schools and universities, but organizations that use the curriculum to impart knowledge can apply for ISO 21001 certification. ISO 21001 Certification for Educational Organization Management System (EOMS) follows 11 principles. These are:
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Service Duration | One Month |
Service | Online |
Payment | Online |
Application | ISO Certificate |
Deals | PAN India |
SO 37001 follows the High-Level Structure (HLS) and shares the common terminology with other management system standards developed by ISO. This means that an ABMS can either be established as a stand-alone management system, be part of an overall compliance management system based on ISO 37301, or be integrated with other management systems based on standards such as ISO 37002, ISO 9001, and ISO 45001.
ISO 37001 benefits to organizationsImplementing an ABMS based on ISO 37001 can be a good strategic decision to demonstrate an organization’s commitment to effectively prevent, detect, and respond to bribery. Organizations seeking an effective ABMS will have to demonstrate their commitment to prevent bribery by establishing policies, procedures, and controls which contribute in reducing bribery risks. Nevertheless, the requirements of ISO 37001 are generic; therefore, organizations will have plenty of freedom to establish an ABMS which best suits their needs.
Some of the benefits that organizations would obtain by implementing an ABMS based on ISO 37001 include:
ISO 37001:2016 specifies requirements and provides guidance for establishing, implementing, maintaining, reviewing and improving an anti-bribery management system. The system can be stand-alone or can be integrated into an overall management system. ISO 37001:2016 addresses the following in relation to the organization's activities:
· bribery in the public, private and not-for-profit sectors;
· bribery by the organization;
· bribery by the organization's personnel acting on the organization's behalf or for its benefit;
· bribery by the organization's business associates acting on the organization's behalf or for its benefit;
· bribery of the organization;
· bribery of the organization's personnel in relation to the organization's activities;
· bribery of the organization's business associates in relation to the organization's activities;
· direct and indirect bribery (e.g. a bribe offered or accepted through or by a third party).
ISO 37001:2016 is applicable only to bribery. It sets out requirements and provides guidance for a management system designed to help an organization to prevent, detect and respond to bribery and comply with anti-bribery laws and voluntary commitments applicable to its activities.
Minimum Order Quantity | 5 Certificate |
Service Location | Pan India |
Service Mode | Online |
Payment Mode | Online |
Duration | Same Day |
Service Type | ISO 22000:2018 Certification Service |
This document specifies requirements for a food safety management system (FSMS) to enable an organization that is directly or indirectly involved in the food chain:
a) to plan, implement, operate, maintain and update a FSMS providing products and services that are safe, in accordance with their intended use;
b) to demonstrate compliance with applicable statutory and regulatory food safety requirements;
c) to evaluate and assess mutually agreed customer food safety requirements and to demonstrate conformity with them;
d) to effectively communicate food safety issues to interested parties within the food chain;
e) to ensure that the organization conforms to its stated food safety policy;
f) to demonstrate conformity to relevant interested parties;
g) to seek certification or registration of its FSMS by an external organization, or make a self-assessment or self-declaration of conformity to this document.
All requirements of this document are generic and are intended to be applicable to all organizations in the food chain, regardless of size and complexity. Organizations that are directly or indirectly involved include, but are not limited to, feed producers, animal food producers, harvesters of wild plants and animals, farmers, producers of ingredients, food manufacturers, retailers, and organizations providing food services, catering services, cleaning and sanitation services, transportation, storage and distribution services, suppliers of equipment, cleaning and disinfectants, packaging materials and other food contact materials.
This document allows any organization, including small and/or less developed organizations (e.g. a small farm, a small packer-distributor, a small retail or food service outlet) to implement externally-developed elements in their FSMS.
Internal and/or external resources can be used to meet the requirements of this document.
ISO 22000 sets out the requirements for a food safety management system and can be certified to it. It maps out what an organization needs to do to demonstrate its ability to control food safety hazards in order to ensure that food is safe. It can be used by any organization regardless of its size or position in the food chain.
ISO 22000 is a food safety management system by the International Organization for Standardization (ISO) which is outcome focused,[1] providing requirements for any organization in the food industry with objective to help to improve overall performance in food safety. These standards are intended to ensure safety in the global food supply chain. The standards involve the overall guidelines for food safety management and also focuses on traceability in the feed and food chain.
Food safety refers to all those hazards, whether chronic or acute, that may make food injurious to the health of the consumer.[2]ISO 22000 standard[edit]
ISO 22000 is the most popular voluntary food safety international standard in the food industry with 51,535 total number of sites (as per the ISO Survey 2022). The ISO 22000 family are international voluntary consensus standards which align to Good Standardization Practices (GSP)[3] and the World Trade Organization (WTO) Principles for the Development of International Standards.[4] Defining the requirements for a Food Safety Management System (FSMS) and incorporating the following elements which as defined as FSMS principles:
Minimum Order Quantity | 5 Certificate |
Service Location | Pan India |
Service Type | ISO 31000:2018 Certification Service |
Service Mode | Online |
Payment Mode | Online |
Duration | Same Day |
ISO 31000 provides principles and generic guidelines to assist organizations in establishing, implementing, operating, maintaining and continually improving their risk management framework.
It is not specific to any industry or sector, so it can be used by any public, private or community enterprise, association, group or individual. This standard can be applied throughout the life of an organization, and to a wide range of activities, including strategies and decisions, operations, processes, functions, projects, products, services and assets.
This standard is not intended to promote uniformity of risk management across organizations. The design and implementation of risk management plans and frameworks will need to take into account the varying needs of a specific organization, its particular objectives, context, structure, operations, processes, functions, projects, products, services, or assets and specific practices employed.
ISO 31000 is organized into the following main clauses:
Clause 3: Principles
Clause 4: Framework
Clause 5: Process
Each of these key activities is listed below.
In order to have an effective risk management, an organization has to comply with these 11 principles.
ISO 31000 states that the success of risk management will depend on the effectiveness of the management framework providing the foundations and arrangements what will embed it throughout the organization at all levels.
The framework:
This clause describes the necessary components of the framework for managing risk and the way in which they interrelate in an iterative manner.
Design of framework for managing risk: Before the implementation, the organization must design a framework for managing risk. This includes:
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Minimum Order Quantity | 5 Certificate |
Payment Mode | Online |
Duration | Same Day |
Service Type | ISO 45001:2018 Certification Service |
Service Location | Pan India |
Service Mode | Online |
ISO 45001:2018
ISO 45001 is an international standard that specifies requirements for an occupational health and safety (OH&S) management system. It provides a framework for organizations to manage risks and improve OH&S performance.
The standard establishes criteria for an OH&S policy, objectives, planning, implementation, operation, auditing and review. Key elements include leadership commitment, worker participation, hazard identification and risk assessment, legal and regulatory compliance, emergency planning, incident investigation and continual improvement.
ISO 45001 utilizes the Plan-Do-Check-Act methodology to systematically manage health and safety risks. It applies to organizations of all sizes and can be integrated with other ISO management system standards.
Why is ISO 45001 important?Implementing ISO 45001 provides significant value to organizations looking to reduce workplace incidents and demonstrate OH&S commitment. Benefits include:
In summary, ISO 45001 enables organizations to better protect their workers and manage OH&S risks, making it an essential standard worldwide.
Benefits
Service Location | Pan India |
Service Mode | Online |
Payment Mode | Online |
Duration | 15 Days |
Delivery Time | SAME DAY |
The vaccine supply chain involves not only manufacturing the vaccine contents, but also using temperature-controlled storage to help maintain vaccine quality from production to patient.
To engender confidence in their choice of products for use in immunization programs, UN member states and purchasing agencies may rely on the WHO Performance, Quality and Safety (PQS) process. PQS prequalifies devices for use based on performance relative to applicable standards, quality and reliability characteristics needed for use in challenging environments and safety characteristics that protect people and the environment throughout the course of the product's life cycle.
Products that have been tested and found to meet the applicable specification standards are listed in the WHO PQS Devices Catalogue, which includes information aimed at helping purchasers make informed choices.
Minimum Order Quantity | 5 Certificate |
Service Location | Pan India |
Service Mode | Online |
Payment Mode | Online |
Duration | Same Day |
Service Type | ISO 37001:2016 Certification Service |
SO 37001 follows the High-Level Structure (HLS) and shares the common terminology with other management system standards developed by ISO. This means that an ABMS can either be established as a stand-alone management system, be part of an overall compliance management system based on ISO 37301, or be integrated with other management systems based on standards such as ISO 37002, ISO 9001, and ISO 45001.
ISO 37001 benefits to organizationsImplementing an ABMS based on ISO 37001 can be a good strategic decision to demonstrate an organization’s commitment to effectively prevent, detect, and respond to bribery. Organizations seeking an effective ABMS will have to demonstrate their commitment to prevent bribery by establishing policies, procedures, and controls which contribute in reducing bribery risks. Nevertheless, the requirements of ISO 37001 are generic; therefore, organizations will have plenty of freedom to establish an ABMS which best suits their needs.
Some of the benefits that organizations would obtain by implementing an ABMS based on ISO 37001 include:
ISO 37001:2016 specifies requirements and provides guidance for establishing, implementing, maintaining, reviewing and improving an anti-bribery management system. The system can be stand-alone or can be integrated into an overall management system. ISO 37001:2016 addresses the following in relation to the organization's activities:
· bribery in the public, private and not-for-profit sectors;
· bribery by the organization;
· bribery by the organization's personnel acting on the organization's behalf or for its benefit;
· bribery by the organization's business associates acting on the organization's behalf or for its benefit;
· bribery of the organization;
· bribery of the organization's personnel in relation to the organization's activities;
· bribery of the organization's business associates in relation to the organization's activities;
· direct and indirect bribery (e.g. a bribe offered or accepted through or by a third party).
ISO 37001:2016 is applicable only to bribery. It sets out requirements and provides guidance for a management system designed to help an organization to prevent, detect and respond to bribery and comply with anti-bribery laws and voluntary commitments applicable to its activities.
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Minimum Order Quantity | 5 Certificate |
Service Location | Pan India |
Service Mode | Online |
Payment Mode | Online |
Duration | Same Day |
Service Type | ISO 17025:2017 General Certification Service |
ISO/IEC 17025:2017 is an international standard specifying requirements for quality and competence in testing and calibration laboratories. The standard requires that such labs prioritise excellent quality practices and develop a reliable quality management system to establish and demonstrate their competence.
The full standard is called ISO/IEC 17025, since the certification was created by the International Organization for Standardization in conjunction with the International Electrotechnical Commission. However, many shorten this to ISO 17025 or simply 17025 certification when referring to the standard.
Ultimately, ISO 17025 is for any organization that performs testing, sampling or calibration and wants to be sure of the reliability of their results. The simplest way we can put it: if you work in a testing environment that produces measurable results, then ISO 17025 is probably applicable. This may even mean you don’t necessarily call your facility a “lab,” but by ISO standards, you would be considered a laboratory if you are producing measurable results.
ISO/IEC 17025 is applicable to many different testing and calibration facilities across a range of sectors. The forensics sector is an example of one area that has almost universally adopted ISO/IEC 17025 as the main indicator of quality in its labs. But laboratories in sectors as diverse as asbestos testing, acoustics, chemicals, fibre optics, food production, textiles, and even cannabis labs are certified to ISO 17025 standards.
Medical laboratories are one slight exception. Labs looking for an internationally recognised standard of quality in medical labs should look into ISO 15189 certification, as this is the standard that applies specifically to med labs. If you work in a medical lab, for example a pathology lab or in a clinical trial environment, you will find all the information you need about ISO 15189 in our dedicated knowledge hub.
ISO 17025 is of high importance for testing and calibration labs because it is globally recognized. Accreditation allows you to ensure and demonstrate the reliability of your results as well as the integrity, competence, and overall quality of your lab’s practices. It also includes demands for proficiency testing, which serves as another clear indicator of your lab’s competence. We discussed proficiency testing and its importance as part of ISO 17025 in a recent webinar.
It can be crucial to the perception of your organization as credible, trustworthy and competent to current and potential customers or business partners. That’s without even mentioning the fact that many government organisations around the world will have such accreditation as a strict prerequisite before looking to work with you.