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Is 2713 5 6 Meter Tubular Pole
75,000 Per CERTIFICATE
The tubular steel poles shall conform to the latest edition of Indian Standard specifications IS- 2713 (Part-I-II):1980 (amended up-to date) except where specified otherwise in this specification.
Material : Mild Steel
Certificate : YES
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IS 2415 Cycles - Rubber Tubes
75,000 Per CERTIFICATE
This Indian standard was adopted by BIS after the draft finalized by the bicycles section committee had been approved by the transport engineering division council.
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usb driven barcode readers bis registration
17,000 - 18,000 Per certificate
USB (Universal Serial Bus) Barcode Scanners use a PC computer's USB port to move or sync captured data. USB also supports hot-plugging, which allows you to plug and unplug scanners without having to restart your computer. USB ports can be found on computer desktops, laptops, and certain cell phone models. Because USB ports are directly connected to computers, scanning an item's barcode with a USB barcode scanner allows the information to be instantly transmitted to a computer database or programme. USB scanners can connect to both Android and iOS devices, making portable scanning quick and easy. The Government of India and Bureau of Indian Standards (BIS) have required BARCODE READERS to be registered as per IS 13252 (Part 1):2010 under the Compulsory Registration Scheme from BIS. BIS Registration is a must for both domestic and foreign manufacturers in order to sell products in the Indian market otherwise, it will be a punishable offence.
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TELEVISION OTHER THAN PLASMA/LCD/LED TVS - IS 616: 2017
17,000 - 18,000 Per RS
Television is also known as TV. The most obvious use of your television is, of course, watching it, whether it's the news, your favorite soap opera, or the latest hit drama or movie. This is the primary function of television and the purpose for its huge success. The term applies to a television set, a TV show, or the medium used to transmit television signals. Television is a popular mass-media way to advertising, entertainment, news, and sports. We depend on TV for leisure, news, education, weather forecast news, sports, culture, and even music since the beginning of music videos. As Television is an electronic device mostly used in every home, keeping this in consideration, the Government of Indian and Bureau of Indian Standards has taken a step that it is compulsory for the manufacturers to register television under Compulsory registration scheme as per IS 616: 2017. BIS have mentioned all terms and condition in the Indian Standards IS 616:2017 and must be manufactured as per the Indian Standard. It opens all the doors to the manufacturer for export/import, manufacture, sell and distribute in Indian Market.
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ROHS Certification Service
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 CERTIFICATION Polybrominated Diphenyl Ethers (PBDE) Polybrominated Biphenyls (PBB) Hexavalent Chromium (CrVI) Cadmium (Cd) Mercury (Hg) Lead (Pb) EXEMPTED PRODUCTS UNDER ROHS CERTIFICATION Military and National Defense products Products that do not rely on electricity as their major source of energy Products whose primary function does not necessitate the use of electricity Sub-assembly or component of an exempted product category Products that support micro, small, and medium-sized manufacturing and service firms, as defined by the Micro, Small, and Medium-Sized Enterprises Development Act of 2006. Batteries Radioactive waste RoHS Certification Services Intertek 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: Declarations of Conformity (DoC) Test reports Materials declarations from the suppliers of materials and/or components 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: A trusted third-party partnership in RoHS self declaration Assurance that products and accompanying documentation has been independently reviewed and certified by a competent third party
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recessed led luminaires bis registration
17,000 - 18,000 Per RS
Recessed LED Luminaries are the LED light fixture which is installed into the hollow opening of the surface whether it’s on the ceiling or on another surface. It includes 3 main fixtures that are bulb, trim, and housing. The housing is the majority of the fixture that is buried within the wall or ceiling and houses the fixture's electrical connections. Trim refers to the attractive, visible component of the fixture, which may incorporate baffles, reflectors, or shades. The last component is the bulb, which is the component of the fixture that generates light. The lights are very sleek, easily fit anywhere in less space, and illuminates the whole area. These lights are great for the kitchen, closets, shower stalls, and anywhere there are low ceilings. As recessed lights are electric in nature, so it is compulsory to register recessed LED Luminaries under BIS Registration as per IS 10322 (Part 5/Section 2): 2012 under Compulsory Registration Scheme from BIS. It is compulsory for the domestic as well as the foreign manufacturers to register recessed LED Luminaries under compulsory registration scheme or BIS registration otherwise it will be a punishable offense.
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PCI DSS Compliance Service
What is the purpose of PCI DSS? The primary goal of PCI DSS is to safeguard and optimize the security of sensitive cardholder data, such as credit card numbers, expiration dates and security codes. The standard's security controls help businesses minimize the risk of data breaches, fraud and identity theft. Compliance with PCI DSS also ensures that businesses adhere to industry best practices when processing, storing and transmitting credit card data. In turn, PCI DSS compliance fosters trust among customers and stakeholders. What are the 6 principles of PCI DSS? The PCI Security Standards Council (PCI SSC) has created six major goals for PCI DSS: Build and maintain a secure network and systems. Credit card transactions must be conducted in a secure network. The security infrastructure should include firewalls that are strong and complex enough to be effective without causing inconvenience to cardholders or vendors. Specialized firewalls are available for wireless local area networks, which are highly vulnerable to eavesdropping and malicious attacks. Vendor-provided authentication data, such as personal identification numbers and passwords, should not be used on an ongoing basis. Protect cardholder data. Organizations adhering to PCI DSS must protect cardholder information wherever it's stored. Repositories with vital data, such as birthdates, mothers' maiden names, Social Security numbers, phone numbers and mailing addresses, must be secure. The transmission of cardholder data through public networks must be encrypted. Maintain a vulnerability management program. Card services organizations must institute risk assessment and vulnerability management programs that protect their systems from the activities of malicious hackers, such as spyware and malware. All applications should be free of bugs and vulnerabilities that might enable exploits in which cardholder data could be stolen or altered. Software and operating systems must be regularly updated and patched. Implement strong access control measures. Access to system information and operations should be restricted and controlled. Every person who uses a computer in the system must be assigned a unique and confidential identification name or number. Cardholder data should be protected physically, as well as electronically. Physical protection can include the use of document shredders, limits on document duplication, locks on dumpsters and security measures at the point of sale. Regularly monitor and test networks. Networks must be regularly monitored and tested to ensure security measures are in place, functioning properly and up to date. For example, antivirus and antispyware programs should be provided with the latest definitions and signatures. These programs frequently scan all exchanged data, applications, RAM and storage media. Maintain an information security policy. A formal information security policy must be defined, maintained and followed by all participating entities. Enforcement measures, such as audits and penalties for noncompliance, might be necessary. What are the requirements of PCI DSS? PCI SSC includes specific requirements in each of the six PCI DSS goals. Organizations that want to be PCI DSS-compliant must meet these 12 requirements: Install and maintain a firewall to protect cardholder data environments. Don't use vendor-supplied default passwords and other security parameters. Protect stored cardholder data. Encrypt payment card data transmitted across open, public networks. Use and regularly update antivirus software. Develop and maintain secure systems and applications. Restrict access to cardholder data to employees with a business need because their jobs require access..
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Management System Certification Service
The WHO Performance, Quality and Safety (PQS) process 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.
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ISO IEC 27001:2022 Certification Service
ISO/IEC 27001 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. Benefits Resilience to cyber-attacks Preparedness for new threats Data integrity, confidentiality and availability Security across all supports Organization-wide protection Cost savings Confidentiality→ Meaning: Only the right people can access the information held by the organization.⚠ Risk example: Criminals get hold of your clients’ login details and sell them on the Darknet. Information integrity→ Meaning: Data that the organization uses to pursue its business or keeps safe for others is reliably stored and not erased or damaged.⚠ Risk example: A staff member accidentally deletes a row in a file during processing. Availability of data:→ Meaning: The organization and its clients can access the information whenever it is necessary so that business purposes and customer expectations are satisfied.⚠ Risk example: Your enterprise database goes offline because of server problems and insufficient backup. An 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. Reduce your vulnerability to the growing threat of cyber-attacks Respond to evolving security risks Ensure that assets such as financial statements, intellectual property, employee data and information entrusted by third parties remain undamaged, confidential, and available as needed Provide a centrally managed framework that secures all information in one place Prepare people, processes and technology throughout your organization to face technology-based risks and other threats Secure information in all forms, including paper-based, cloud-based and digital data Save money by increasing efficiency and reducing expenses for ineffective defence technology
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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: Customer confidence: The standard ensures that organizations have robust quality control processes in place, leading to increased customer trust and satisfaction. Effective complaint resolution: ISO 9001 offers guidelines for resolving customer complaints efficiently, contributing to timely and satisfactory problem-solving. Process improvement: The standard helps identify and eliminate inefficiencies, reduce waste, streamline operations, and promote informed decision-making, resulting in cost savings and better outcomes. Ongoing optimization: Regular audits and reviews encouraged by ISO 9001 enable organizations to continually refine their quality management systems, stay competitive, and achieve long-term success. Benefits of ISO 9001 Increased customer trust and satisfaction Sound quality control processes Cost savings and productivity gains Culture of continuous improvement
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ISO 45001:2018 Certification Service
ISO 45001:2018ISO 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: ISO 45001 provides an internationally-recognized framework for managing occupational health and safety risks. It enables organizations to systematically assess hazards and implement risk control measures, leading to reduced workplace injuries, illnesses and incidents. Adopting the standard shows employees and external stakeholders that the organization is committed to worker health, safety and wellbeing. This boosts reputation, morale and retention. The standard requires complying with OH&S regulations, ensuring legal conformity. It also promotes proactive risk management, potentially lowering insurance premiums. By requiring emergency preparedness and response protocols, ISO 45001 strengthens organizational resilience against safety threats and crises. The framework of plan, do, check act means the OH&S system can continually improve and evolve, enhancing long-term worker health and safety performance. In summary, ISO 45001 enables organizations to better protect their workers and manage OH&S risks, making it an essential standard worldwide. Benefits Framework to systematically manage OH&S risks Reduced workplace incidents and injuries Demonstrated commitment to worker health and safety Ensured compliance with OH&S regulations Increased organizational resilience Continual improvement of OH&S performance
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ISO 3834-1:2021 Certification Service
ISO 3834 is regarded as the welding quality requirement benchmark of the 21st century and certified compliance means global recognition of a company's capabilities. The ISO 3834 standard is a tool for the control of the entire welding process from design to final handover. 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 arePart 2: Comprehensive quality requirementsPart 3: Standard quality requirementsPart 4: Production requirementsPart 5: The documents with which it is necessary to conform to claim to the quality requirements of EN ISO 3834-2,3,4Part 6: Guidelines for implementing ISO 3834Special 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.
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ISO 37001:2016 Certification Service -
An ABMS based on ISO 37001 is intended to help organizations effectively prevent, detect, and respond to bribery. Other forms of corruption, such as fraud, are not covered by the standard. The requirements of the standard are generic and applicable to all organizations, regardless of their type, size, and sector (public, private, or not-for-profit). Furthermore, ISO 37001 can be used to tackle bribery by or of the organization as well as direct and indirect bribery. 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 organizations Implementing 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: Improved ability to detect, prevent, and respond to bribery by or of the organization Opportunity to certify the ABMS by undergoing a conformity assessment from an accredited conformity assessment body Establishment of processes that allow proper due diligence of prospective personnel and business associates Opportunity to contribute in the global fight against bribery Opportunity to shape, improve, or transform the culture of an organization Improved ability to respond, mitigate, and deal with the consequences if a bribery case occurs In certain jurisdictions, the existence of an internal mechanism to address bribery issues can reduce penalties in cases of wrongdoing 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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ISO 31000:2018 Certification Service
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. Clause 3: Principles of risk management In order to have an effective risk management, an organization has to comply with these 11 principles. Risk management creates and protects value; Risk management is an integral part of all organizational processes; Risk management is part of decision making; Risk management explicitly addresses uncertainty; Risk management is systematic, structured and timely; Risk management is based on the best available information; Risk management is tailored; Risk management takes human and cultural factors into account; Risk management is transparent and inclusive; Risk management is dynamic, iterative and responsive to change; Risk management facilitates continual improvement of the organization. Clause 4: Framework 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: assists in managing risks effectively through the application of the risk management process; ensures that information about risk derived from the risk management process is adequately reported; and ensures that these information is used as a basis for decision making and accountability at all relevant organizational levels. 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: Understanding of the organization and its context Establishing risk management policy Ensuring accountability, authority and appropriate competence for risk management Integrating risk management into organizational processes Allocating appropriate resources Establishing internal and external communication and reporting mechanisms ISO 31000 states that the success of risk management will depend on the effectiveness of the management The risk management process should be: An integral part of management; Embedded in the culture and practices; Tailored to the business processes of the organization. Risk management process comprises the following activities:
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ISO 22000:2018 Certification Service
ISO 22000:2018 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[edit] 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: system management prerequisite programs HACCP principles
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ISO 21001:2018 Certification Service
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. Which Educational Organizations can apply for ISO 21001 Certification? 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: Pre-schools Colleges Adult Education Centers Vocational Education Centers Tutoring or Coaching Centers Training Institutes Special Education Schools Universities K-12 Schools Principles of ISO 21001 Certification 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: Focus on learners and other beneficiaries – It promotes student-centred learning and focuses on the needs and requirements of individual learners. Visionary leadership – It focuses on engaging all learners and defines competence standards for all staff to achieve the mission, vision and objectives of the organization. Engagement of people – It aims to provide training and develop competence to ensure that all the people involved are empowered, competent and engaged in delivering values. Process approach – It aims to establish a coherent system to achieve consistent and predictable results. It reviews processes and focuses on adopting efficient and effective processes to improve the functioning of the organizations. Improvement – It follows the principle of continual improvement to sustain growth and eliminates factors that might cause unintended outcomes. Evidence-based decisions – Decisions are based on analysis and evaluation after reading the prior information and data to achieve the intended outcomes. Relationship Management – It is equally necessary for an organization to maintain a relationship with customers, stakeholders and other beneficiaries to sustain growth. Social Responsibility – An organization must behave in a socially responsible manner to ensure long-term success and sustainable growth. The International Organization for Standardization (ISO) has developed ISO 26000 certification solely dedicated to Social Responsibility.
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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. Who is ISO/IEC 17025 for? 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. Benefits of ISO/IEC 17025 Establishes a global benchmark for laboratory quality and reliability Enhances confidence in test and calibration results, both domestically and internationally Facilitates cooperation between laboratories and other bodies by generating wider acceptance of results Reduces the need for retesting, saving time and resources
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ISO 14855-1:2012 Certification Consultancy Service
Our ISO 14855-1:2012 Certification Consultancy Service ensures a streamlined process for environmental biodegradability testing. Our expert consultants guide your organization through the certification requirements, offering comprehensive assistance in protocol implementation, documentation, and audit preparation. We focus on aligning your practices with ISO 14855-1 standards, emphasizing environmentally responsible practices. Our service encompasses detailed training sessions, documentation review, and continuous support to guarantee a successful certification process. By choosing our consultancy, you gain a partner dedicated to enhancing your environmental footprint and ensuring compliance with ISO 14855-1:2012, fostering a commitment to sustainable and eco-friendly practices within your business.
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ISO 14001:2015 Certification Service
ISO 14001:2015Environmental management systems 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. Benefits Enhanced environmental performance Regulatory compliance Risk management Cost savings Operational excellence Stakeholder and customer trust
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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 Devices A 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: Surgical instruments Wheelchairs Hospital beds CT scanners Catheters Defibrillators Understanding ISO 13485 Certification 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 Businesses Organizations 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 Requirements To 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. Benefits of ISO 13485 Certification Improvement in quality and safety of medical devices. Reduction in operational errors and waste. Demonstration of compliance with local regulations. Enhancement of customer confidence and satisfaction. Strengthening relationships with stakeholders. Creation of new global business opportunities. Application/Contract Review: 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
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ISO 10001:2018 Certification Service
ISO 10002 Customer Satisfaction. Complaints Handling 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? Achieve operational efficiency to identify trends and causes of complaints Resolve more complaints by adopting a more customer-focused approach Engage staff with new customer service training opportunities Integrate ISO 10002 with ISO 9001 to improve overall efficiency Monitor and continually improve your complaints handling process. Implementing ISO 10001 customer complaints 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. Top tips for implementing ISO 10002 Get commitment and support from senior management. Engage the whole business with good internal communication. Compare existing management processes with ISO 10002 requirements. Get customer feedback on current complaints management. Establish an implementation team to get the best results. Map out and share roles, responsibilities and timescales. Adapt the principles of ISO 10002 management systems to your business. Motivate staff involvement with training and incentives. Train staff to understand and use the ISO 10002 management system. Regularly review your ISO 10002 system to make sure it remains effective and that you are continually improving it.
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IEC 61010-1:2010 Safety Requirement Certification Service
IEC 61010-1:2010 specifies general safety requirements for the following types of electrical equipment and their accessories, wherever they are intended to be used.a) Electrical test and measurement equipmentb) Electrical industrial process-control equipment c) Electrical laboratory equipmentThis third edition cancels and replaces the second edition published in 2001. It constitutes a technical revision. This edition includes the following significant changes from the second edition, as well as numerous other changes.- The scope of the standard has been expanded to include all locations where these products may be used, so that both professional and non-professional versions of these products are within the scope.- The requirements for testing and measuring circuits (in various subclauses and the entirety of Clause 16) have been removed and included in a particular standard IEC 61010-2-030.- Insulation requirements (6.7) have been completely rewritten.- Additional requirements for protection against mechanical HAZARDS (Clause 7) have been included.- Surface temperature limits (Clause 10) have been modified to conform to the limits of EN 563.- Radiation requirements (Clause 12) have been modified, and take into account a distinction between intended emission and unintended emission.- Requirements for reasonably foreseeable misuse and ergonomic aspects have been added (Clause 16).- A new clause (Clause 17) has been added to deal with HAZARDS and environments not covered by the standard, along with a new informative annex (Annex J) dealing with RISK assessment.- A new informative annex (Annex E) addresses methods of reducing the POLLUTION DEGREE of a micro-environment.- Requirements for the qualification of coatings for protection against POLLUTION have been added (Annex H).- A new informative annex (Annex I) has been added to further explain how to determine the WORKING VOLTAGE of a MAINS CIRCUIT.The contents of the corrigendum 1 of May 2011, the interpretation sheet 1 of February 2013 and the corrigendum 2 of October 2013 have been included in this copy. What is IEC 61010? 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: Medical laboratory equipment Electrical medical equipment Test and measurement instruments Industrial process control equipment Electrical test equipment Automatic control systems 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 61010 Compliance 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.
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halal certification service
Halal Certification 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 India In 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 Certification The 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 way The benefits of obtaining a Halal Certificate in India are numerous. Here are some of the key benefits: Access to a growing market: By obtaining a Halal Certificate, businesses can tap into this growing market and reach a wider audience. Increased consumer trust and confidence: By obtaining a Halal Certificate, businesses can demonstrate to Muslim consumers that their products or services meet these standards, which can help build trust and confidence in the brand. Compliance with regulatory requirements: Some states in India, such as Kerala and Tamil Nadu, require Halal Certification for specific products or services to be sold in their markets. By obtaining a Halal Certificate, businesses can ensure that their products or services meet regulatory requirements and avoid legal or regulatory issues. Global recognition: Halal Certification in India is recognized worldwide, and obtaining this Certification can help businesses expand into international markets where Halal products and services are in high demand. Competitive advantage: A Halal Certificate can give businesses a competitive edge over other companies that do not have this Certification. Businesses having this Certification can make a business more appealing to them.
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haccp certification service
HACCPHazard Analysis Critical Control Points (HACCP) is a system which provides the framework for monitoring the total food system, from harvesting to consumption, to reduce the risk of foodborne illness. The system is designed to identify and control potential problems before they occur. In its Model Food Code, the Food and Drug Administration has recommended the HACCP system “because it is a system of preventive controls that is the most effective and efficient way to assure that food products are safe ” (1999 FDA Model Food Code) . The application of HACCP is based on technical and scientific principles that assure safe food.haccp terminology Critical Control Point (CCP) – A procedure/practice (control) in food handling/preparation that will reduce, eliminate or prevent hazards. It is a “kill” step that kills microorganisms or a control step that prevents or slows their growth. Hazard – Unacceptable contamination, microbial growth, persistence of toxins or survival of microorganisms that are of a concern to food safety. Monitoring – Checking to determine if the criteria established by the critical control point(s) (CCP) have been achieved. Risk – Probability that a condition(s) will lead to a hazard.Severity – Seriousness of the consequences of the results of a hazard. ractical haccp principles Practical HACCP principles adapt the seven HACCP steps into a form that is easily applied in a non commercial setting. The seven steps deal with the issues of thorough cooking and cooling which are the major causes of foodborne illness. In order for this simplified, focused application of HACCP principles to be effective in reducing the risk of foodborne illness, Standard Operating Procedures (SOP’s) of personal hygiene, basic sanitation and food storage must be developed and adhered to. The SOP’s should be developed, taking into consideration the types of foods that will be prepared during the foods labs, the number of students involved in the food preparation activity and the type of equipment to be used. The SOP’s can be listed in the form of a checklist, which can be checked off as each item is accomplished.formal haccp seven steps 1. Conduct a hazardous analysis.The purpose of a hazardous analysis is to develop a list of hazards which are likely to cause injury or illness if they are not controlled. Points to be considered in this analysis can include: skill level of employees; transport of food; serving elderly, sick, very young children, immune-compromised; volume cooling; thawing of potentially hazardous foods; high degree of food handling and contact; adequacy of preparation and holding equipment available; storage, and method of preparation. The next step is to determine if the factors may influence the likely occurrence and severity of the hazard being controlled. Finally, the hazards associated with each step in the flow of food should be listed along with the measures necessary to control the hazard. At this step in preparation can food become contaminated and/or can contamination increase? Can this hazard be prevented through corrective action(s)? Can this hazard be prevented, eliminated or reduced by steps taken later in the preparation process? Can you monitor the CCP? How will you measure the CCP? Can you document the CC
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Greenguard Certification Service
Indoor air quality is a crucial aspect of our health and well-being, especially in a world where we spend most of our time indoors. As a result, many individuals and organizations are taking steps to ensure that the products and materials we use in our indoor spaces are safe and have low chemical emissions. This is where Green Guard Certification comes in. In India, this certification has become increasingly popular, allowing manufacturers to create and buyers to identify products that meet strict environmental standards. Let’s explore the importance of Green Guard Certification and how it’s helping to create a safer and healthier indoor environment in India.I. Introduction 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.
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GMP Certification Service
GMP (Good Manufacturing Practice) is the part of quality assurance that ensures consistent quality standards in the production and testing of medicinal products or active ingredients (APIs). This is a short excerpt from the eLearning course on GMP basics Human health is the primary concern. In everyday life, patients must feel they can rely on the high quality of a medicinal product, as they cannot check this themselves. The quality of a medicinal product is determined above all by the following factors: Identity (are the specified ingredients contained?) Content (are the ingredients present in the specified quantity?) Purity (is the product free of ingredients that do not belong in it?) The EU Guidelines to Good Manufacturing Practice require that “The holder of a Marketing Authorisation must manufacture medicinal products so as to ensure that they are fit for their intended use, comply with the requirements of the Marketing Authorisation or Clinical Trial Authorisation, as appropriate and do not place patients at risk due to inadequate safety, quality of efficacy.”This must be proven to the competent authority, which grants approval for the medicinal product, because: without marketing authorisation, a medicinal product may not be marketed to patients. How can these requirements therefore be met? And: how can consistent quality be ensured if it is not possible to individually test each tablet that is pressed? This is the purpose of good manufacturing practice.The principles of good manufacturing practice apply to almost all areas of a company, from research and development to production, quality control, storage and distribution. Anyone who manufactures, tests, stores or markets medicinal products or APIs on a commercial basis must therefore implement a series of defined requirements. The basic principle is that companies must manufacture medicines in such a way that they are suitable for their intended use. The basis for GMP requirements is the CGMP (Current Good Manufacturing Practice) Guide, which the U.S. Food & Drug Administration (FDA) published in the Federal Register in 1978. With this, the authority had created the world's first legally anchored GMP regulations. These made it possible for the manufacturing processes of pharmaceutical companies to be monitored by a regulatory authority. However, the topic also gained importance internationally: In Germany, for example, the German Medicines Act (AMG) was published in 1978 as a direct result of the thalidomide scandal. However, it did not yet contain any specific GMP requirements. It was not until 1985 that the “Pharma-Betriebsverordnung” was published. For the first time, this contained concrete GMP specifications for Germany, which formed the basis for GMP monitoring through inspections by the responsible authorities. It took another four years before the EC GMP Guidelines, which are binding for Europe, finally appeared in 1989. According to the German AMWHV §2, the guideline is now called the EU GMP Guideline and has been legally valid in Germany since 2005, which means that compliance with its specifications must be documented. What are GMP rules?GMP rules are the requirements for quality assurance of the manufacturing processes and environment formulated by the European Commission in the principles and guidelines of Good Manufacturing Practice (GMP) for medicinal products for human use and active pharmaceutical ingredients. The EU GMP Guide describes how these rules are to be interpreted in Part I for medicinal products and in Part II for active substances, as well as in various annexes for specific product groups.
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With e-commerce platforms becoming popular business models having an appropriate quality and certification can help scale your business. It is an ideal way to boost your business sales and marketing to prevent recurring issues. Certification can also help businesses to gain customer trust and aid in higher revenue generation. It provides valuable insight into the risks and business opportunities for better decision-making.
Our company Analyticall Quality Solutions Private Limited is amongst the reputable names in the industry. We are an award-winning certification, registration, and compliance service provider in Uttar Pradesh. We are determined to provide personalized certification services at an economical price in the field of management systems and product certifications.
Our Services
Our company has offered successful services in varying business sectors like health care, manufacturing & engineering, construction, Education, IT, etc. Our team focuses on the ethical measurement, analysis, and improvement using reliable techniques to facilitate varying management systems and product certifications. Our wide range of services includes CMMI certification, Greenguard certification, FCC certification service, etc.
Our experts are dedicated professionals who utilize innovative methods to help satisfy our client\'s quality needs to enhance supplier-customer relationships. Our experts also guide our clients through corrective methods to help enhance quality, functionality, and efficiency for our client\'s business. Our user-friendly platform enables our clients to hire our high–quality certification services from any location hassle-free.
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