ISO 9001 is the international standard for Quality Management System (QMS).
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Organizations use ISO 9001:2015 standard to reveal the consistent ability on products and services that meet customer and regulatory requirements. |
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ISO 9001:2015 Quality Management System continuously enhances the organization and efficiency of the process. |
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QMS is suitable for all businesses like manufacturers, traders, service providers, institutions irrespective of their size. |
QMS is a powerful tool for Business Improvement and Enhanced Customer Satisfaction. It helps to:
Standardize the organization processes Streamline your operations Cut down additional cost expenses Satisfy your customers with timely deliverables Showcase consistency in quality Monitor the performances on Product and Process Efficient supplier management Identify and manage the risks Regulate inventorys Smart house keeping 
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ISO 14001:2015 most recognized Environmental Management System used to enhance the Organizations environment. |
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EMS is part of the management system used to manage environmental aspects, fulfill compliance obligations, and address risks and opportunities. |
ISO 14001:2015 prominently highlights social responsibility of Organization on efficient resource utilization with reduction of waste. Organization works on reduction of cost to attract stakeholders. Largely, it boosts sustainable organizational growth.
Environmental Management System helps organizations identify, manage, monitor and control their environmental issues in a "holistic" manner:
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Enhancement of environmental performance |
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Fulfillment of compliance obligations/legal requirements |
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Achievement of environmental objectives |
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EMS is suitable for all organizations regardless of size, location, sector or industry a private, nonprofit or governmental. |
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ISO 14001:2015 is a benchmark for organizations that cares environmental issues valid its operations. |
EMS is a framework that helps:
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Increase business establishment opportunities and strategic business aims |
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Diminish the risk of pollution incidents |
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Provide assurance that environmental risk been managed |
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Identify cost savings with greater emphasis on resource, waste and energy management |
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Quantify, monitor and control the impact of operations on the luminous environment |
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Ensure legislative awareness and compliance |
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Improve environmental performance of supply chain |
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Protect the company, assets, shareholders and directors |
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Improve Customer trust |
ISO 45001:2018 is the first International Standard on Occupational Health and Safety Management System.
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ISO 45001:2018 predominantly builds strong, healthy and safety workforce environment for your Organization. International Organizations can adhere to single standard OHSMS to practice uniqueness across regions. |
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ISO 45001:2018 provide safe and healthy work places for Organizational workers, visitors, contractors and other interested parties to prevent work-related injury and ill –health irrespective of their background and workforce volume. |
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OHSMS is suitable for all organizations regardless of size, location, sector or industry a private, nonprofit or governmental. |
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ISO 45001:2018 is a benchmark for organizations that cares for operational healthy and safety measures. |
OHSMS is a framework that helps:
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Identify legal requirements without compliance issues |
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Reducing the rate of Incidents or accidents |
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Encouraging leadership among employees, Sense of Ownership |
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Implement safe and healthy workplace to monitor performance threats |
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Implement a system to manage risks and opportunities systematically |
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To improve cultural change |
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Employees work at secure environment across levels, regions and geographical locations |
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Promotes brand reputation |
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IATF 16949:2016 is Automotive Quality Management System, specifically for the automotive sector. |
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Automotive Quality Management System is the combined effort by The International Automotive Task Force (IATF) with International Organization for Standardization (ISO). |
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IATF 16949:2016 is an integration of both IATF 16969 and ISO 9001:2015 Quality Management System. IATF aligns to the standards of Europe and US persuading IATF with International Recognition. |
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IATF is suitable for all organizations in manufacturing or servicing automotive sector or industry, a private or governmental regardless of size, location. |
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IATF 16949:2016 is a benchmark for organizations that cares for reducing waste in supply chain management and ensures safety measures with quality. |
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Identify legal requirements without compliance issues |
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Reducing the defect in by product or parts |
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Reducing the waste in production process |
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Reducing the variant in assembling units |
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Continual improvement in supply chain management |
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Deliver quality product across regions and zones |
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Encouraging leadership among employees, Sense of Ownership |
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Standard safety measures on products across regions and zones |
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Implement a system to manage risks and opportunities systematically |
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Promotes brand reputation |
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Increase stakeholders trust |
ISO 22000 is the international standard for Food Safety Management System (FSMS).
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Organizations use ISO 22000:2018 standard to reveal the consistent safety on food products and services that meet global requirements of customers. |
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ISO 22000:2018 Food Safety Management Systems continuously ensures the safety on food products comply with food safety regulations throughout the world. |
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FSMS is suitable for all food industries much concern on food safety and involved in food chain businesses like bakers, producers, manufacturers, traders, service providers, Transportation, storage, Packaging and retail, irrespective of their size and location. |
FSMS is a powerful tool benchmarking International Business with Enhanced Customer Satisfaction on food products. It helps to:
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Standardize safety measures on food products across regions and zones |
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Standardize the organization processes |
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Streamlined operations |
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Identify and control food safety Hazards |
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Satisfy your customers with timely deliverables |
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Showcase consistency in quality |
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Continual improvement in supply chain management |
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Deliver quality food product across regions and zones |
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Encouraging leadership among employees, Sense of Ownership |
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Implement a system to manage risks and opportunities systematically |
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Promotes brand reputation |
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Increase stakeholders trust |
ISO 13485 is an International Standard for Effective establishment and implementation of Medical Device Quality Management Systems.
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ISO 13485 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements |
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Organizations which are involved in one or more stages of the life-cycle, including design and development, production, storage and distribution, installation, or servicing of a medical device and design and development or provision of associated activities (e.g. technical support) can go for this ISO 13485 implementation. |
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ISO 13485 can also be used by suppliers or external parties that provide product, including quality management system-related services to such organizations. |
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Requirements of ISO 13485 are applicable to organizations regardless of their size and regardless of their type except where explicitly stated. |
Whether your goal is to operate internationally or to expand domestically to accommodate new clients, registration to ISO13485 will help you:
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Execute business in a highly regulated industry. |
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Demonstrate to customers and regulators that you have made a serious commitment to quality for your medical devices. |
ISO/IEC 17025 specifies the general requirements for the competence, impartiality and consistent operation of laboratories.
NABL is a Constituent Board of Quality Council of India. NABL involves in third-party assessment of the technical competence of testing including medical and calibration laboratories, proficiency testing providers and reference material producers.
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ISO/IEC 17025 allows laboratories to implement a sound quality system and demonstrate that they are technically competent and able to produce valid and reliable results. |
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ISO/IEC 17025 also helps facilitate cooperation between laboratories and other bodies by generating wider acceptance of results between countries. Test reports and certificates can be accepted from one country to another without the need for further testing, which, in turn, improves international trade. |
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Testing laboratories |
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Calibration Laboratories |
ISO 27001 is the international standard which is recognized globally for managing risks to the security of information you hold.
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Certification to ISO 27001 allows you to prove to your clients and other stakeholders that you are managing the security of your information. |
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ISO 27001 provides a set of standardized requirements for an Information Security Management System (ISMS). |
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The standard adopts a process based approach for establishing, implementing, operating, monitoring, maintaining, and improving your ISMS. |
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ISO 27001 Certification is suitable for any organisation, large or small, in any sector. The standard is especially suitable where the protection of information is critical, such as in the banking, financial, health, public and IT sectors. |
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The standard is also applicable to organisations which manage high volumes of data, or information on behalf of other organisations such as data centres and IT outsourcing companies. |
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Keeps confidential information secure |
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Provides customers and stakeholders with confidence in how you manage risk |
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Provide continual prevention and assessments of threats within your organization |
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Allows for secure exchange of information |
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Provide you with a competitive advantage |
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Enhanced customer satisfaction that improves client retention |
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Consistency in the delivery of your service or product |
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Manages and minimises risk exposure |
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Builds a culture of security |
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Protects the company, assets, shareholders and directors |
CE Marking is the symbol 
abbreviating the French phrase "Conformité Européene" that means "European Conformity".
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CE marking is a certification mark that indicates conformity with health, safety, and environmental protection standards for products sold within the European Economic Area (EEA). |
CE Marking is required for the Organization who wishes to export their Product to the 27 European Union (EU) and 3 European Free Trade Association (EFTA) member states.
CE Marking is applicable for the following 20 groups of products:
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Appliances Burning Gaseous Fuels (AppliGas) |
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Cableway Installations to Carry Persons |
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Low Voltage Electrical Equipment |
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Construction Products |
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Equipment and Protective Systems for Used in Potentially Explosive Atmospheres (Atex) |
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Explosives for Civil Uses |
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Hot Water Boilers |
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Lift |
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Machinery |
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Measuring Instruments |
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Medical Devices |
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Active Implantable Medical Devices |
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In Vitro Diagnostic Medical Devices |
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Non-automatic Weighing Instruments |
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Radio Equipment & Telecommunications Terminal Equipment (R&TTE) |
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Personal Protective Equipment (PPE) |
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Simple Pressure Vessels |
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Pressure Equipment |
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Recreational Craft |
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Toys |
CE Marking on the product helps to:
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Showcase meeting EC Directives |
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Worldwide recognition |
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Prevent misuse |
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Attract retailers |
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Increases sales export |
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Showcase consumer safe |
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Product marketing simplified in 30 European countries |
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Smooth transition in Customs and Vigilance offices |
Good Manufacturing Practices (GMP) certification ensures the integrity of your food manufacturing process as well as your compliance with food safety regulations
Good manufacturing practices (GMP) includes many basic operational conditions and procedures that are required to be met by the food business. These can include the following:
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The correct construction and layout of the food premises. |
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The condition of the external environment of the food premises. |
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The adequate maintenance of equipment and utensils used within the food business. |
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The use of suitable chemicals within and around the food premises including cleaning chemicals, pest control chemicals and machine lubricants. |
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The identification and storage of waste within and by the food business. |
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The cleanliness of the food premises, equipment, utensils, floors, walls and ceilings. |
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An effective pest control program implemented within the food premises and surrounds. |
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The avoidance of foreign matter within the finished product. Sources of foreign matter can include wood, glass, metal, plastic, pests, paper, string, tape |
GMP is suitable for all Food manufacturers, Food processing industries, Food contact machineries/ materials manufacturers, etc., irrespective of size, location and region. GMP effectively administers and ensures safety across every minute process involved in manufacturing, processing, packing and logistics.
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Good manufacturing practices (GMP) are important in order to produce safe food. |
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The food business has a legal and moral responsibility to produce and prepare food that will not harm the consumer. |
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There can be a high cost to the food business if it does not implement adequate Good manufacturing practices (GMP). |
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All staff should be trained in the food businesses GMP procedures. |
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Assure quality products delivered across regions and zones |
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Ensures reliable and reproducible products |
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Implement a system to manage risks and opportunities systematically |
HACCP is the Hazard Analysis Critical Control Points
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HACCP identifies and controls the entire risk-management processes involved in food products. HACCP focuses on preventing the basic threats in food processing units that eventually built the quality on completed food product. |
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HACCP is key success to food business in international trade. |
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HACCP is suitable for all food industries especially primary producers, manufacturers, processors and food service operators. HACCP effectively administers and ensures food safety across every minute process involved in food chain management. |
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Obtain Internationally reputed food safety on processing system |
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Establishes a high degree of rapport with stakeholders |
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Increases customers inflow |
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Promotes brand reputation |
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Showcase consistency in safety and quality across process |
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Continual improvement in food chain management |
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Continual improvement in supply chain management |
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Deliver quality food product across regions and zones |
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Implement a system to manage risks and opportunities systematically |
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ISO 9001 - (QMS) Quality Management Systems. |
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ISO 14001 - (EMS) Environmental Management Systems |
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ISO 45001 –(OHSMS) Occupational Health and Safety Management Systems |
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ISO 22000 – (FSMS) Food Safety Management System |
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IATF 1649 Automotive Management systems |
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ISO 27001 (ISMS) Information Security Management Systems |
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IMS- Integrated Management Systems to ISO9001, ISO14001 and OHSMS |
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Annual Systems maintenance |
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Auditing Major Project Operations |
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Customer Audit Support – as per OEM Supplier audit criteria / checklist |
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Second Party Audit and Consultancy service |
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ISO 27001 (ISMS) Information Security Management Systems |
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Process Audit |
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Product Audit |
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Process Improvement |
| Standard | Name | Organization | Time Frame for Consultany | Effective from | Earlier Version |
| ISO 9001:2015 | Quality Management System (QMS) | Any Kind of Business – Manufacturers, Traders and service providers | 3 to 6 months | September 2015 | ISO 9001:2008 |
| ISO 14001:2015 | Environmental Management System (EMS) | Concern on Environmental Cause | 5 to 6 months | 2015 | ISO 14001:2015 |
| ISO 45001:2018 | Occupational Health and Safety Management System (OHSMS) | Concern on workforce Health and Safety | 6 to 8 months | March 2018 | OHSAS 18001:2007 |
| IATF 16949:2016 | Automotive Management System (AMS) | Automotive Manufacturing and Servicing Industry | 6 to 8 months | October 2016 | ISO/TS 16949:2009 |
| ISO 22000:2018 | Food Safety Management System (FSMS) | Food Handlers, Manufacturers, Food Packaging manufacturers, Food Machinery Manufacturers | 3 to 6 months | 2018 | ISO 22000:2005 |
| HACCP | Hazard Analysis Critical control Points | Food Processing | 3 to 6 months | 2018 | HACCP |
| CE Marking | European Conformity | Product Manufacturers | 2 to 3 months | 2013 (Based on Directives) | CE Marking |
| GMP | Good Manufacturing Practices | Food & Beverages, Cosmetics, Pharmaceutical Products & Dietary supplements | 3 to 6 months | 2014 –WHO-GMP 2017 US FDA -cGMP | GMP |
| ISO 13485:2016 | Medical devices -- Quality management systems | Medical devices Manufacturers & Service Providers | 6-8 Months | 2016 | ISO 13485:2012 |
| ISO 17025:2017 | Competence of Testing and calibration laboratories | Testing and calibration laboratories | 6-8 Months | 2017 | ISO 17025:2005 |
| ISO 27001:2013 | Information Security Management Systems | Data centres, IT, Banking, Financial, health & Public sectors | 6-8 Months | 2013 | ISO 27001:2005 |
