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ISO22716 International standards for cosmetics
The Standardization Organization (ISO) developed the "ISO22716:2007" standard in November 2007: Cosmetics-Good Manufacturing Practices. This standard provides cosmetic manufacturers with operational guidelines for production, control, storage, and more. The ISO22716 Cosmetic International Standard regulates the management requirements of cosmetics manufacturers; hardware requirements (factory, production site, equipment, etc.), procurement and use of materials, and hygiene and quality control of product manufacturing processes, personnel hygiene management, product inspection, and abnormal quality. Disposal and product complaints and recalls.
Helps you with
Ensure product safety
Improve product quality
Help products enter the international market
Proven business credentials
GMPC (Good Manufacturing Practice Cosmetics)
GMPC (Good Manufacturing PracticeCosmetics) was first promulgated by the US Congress in 1963 to regulate pharmaceutical production. It is also the world's first GMP. The FDA, the US Food and Drug Administration, enacted food GMP in 1980 to regulate food production. In 1992, the FDA issued the Cosmetics GMP Guidelines，to guide cosmetic manufacturers. In order to ensure that the cosmetics produced and sold in its territory (including imported from outside the EU) will not cause harm to consumers' health, the European Union issued the Cosmetics Directive 76/768/EE on July 26, 1976, 2 The seventh edition of the directive was issued on the 27th of the month, and the latest directive requires factories that produce cosmetics to meet good operating practices.
Helps you with
Ensure product safety
Improve product quality
Help products enter the international market
Proven business credentials
1. Overview
ISO45001 is a new occupational health and safety management system standard used by ISO International Standardization Organization to replace OHSAS 18001. The release of ISO 45001 in March 2018 marks an important step in improving occupational health and safety standards worldwide. This new standard is used to help organizations around the world ensure the health and safety of their workers.
An important reason for the emergence of occupational health and safety management system is the need of world economic globalization and international trade development. The basic principle of WTO is "fair competition", which includes environmental and occupational health and safety issues.
Occupational health and safety management system is a management system standard applicable to any organization. The purpose is to reduce and prevent the loss of life, property and time caused by accidents through management.
The construction of ISO 45001 is based on the existing norms of OHSAS 18001. Its main objective is the same, which is to improve the occupational health and safety performance of the organization. At the same time, there are the following differences:
1. Using the advanced structure of ISO management system
2. Pay more attention to the "organizational environment"
3. Emphasize the responsibilities and leadership of top managers
4. Focus more on management responsibilities
5. Emphasis on risk-based thinking
6. Pay more attention to performance monitoring and measurement
2. Benefits from certification
1. Improve the viability of enterprises through risk prevention, innovation and continuous improvement;
2. Enhancing the implementation of occupational health and safety regulations and systems in enterprises;
3. Improving the level of occupational health and safety management in enterprises;
4. Help to eliminate trade barriers;
5. To produce direct and indirect economic benefits to enterprises;
6. Set up the good quality and image of the enterprise, and show the sense of responsibility of the enterprise.
3. Necessary Conditions and List of Information
All kinds of production, trade and service-oriented enterprises registered in the People's Republic of China may apply for certification if they meet the following relevant conditions.
1. Business License
2. Effective certification of qualifications
3. Brief Introduction of Enterprises
4. Organization chart
5. Product process flow chart
6. Planning of plant area
7. Occupational Health and Safety Information
1. Overview
ISO 14001 is the code name of environmental management system certification. ISO 14000 series standards are environmental management system standards formulated by International Organization for Standardization. It is formulated to meet the needs of international environmental protection and to meet the needs of international economic and trade development, aiming at the increasingly serious global environmental pollution and ecological destruction, ozone layer destruction, global warming, the loss of biodiversity and other major environmental problems that threaten human survival and development in the future.
Implementing ISO14001 standard in enterprises is the need of saving energy, reducing consumption, turning waste into treasure, reducing environmental expenditure and reducing cost. Through the establishment and implementation of environmental management system, it can reduce the generation and discharge of pollutants, promote waste recycling, save energy, save raw materials, avoid fines and sewage charges, and reduce costs.
2. Benefits from certification
Establishing the image of the enterprise and enhancing its popularity
Promoting enterprises to consciously abide by environmental laws and regulations
Promote enterprises to consider their impact on the environment in their production, operation, service and other activities and reduce environmental load
Enabling enterprises to obtain "green passes" to enter the international market
Enhancing the environmental awareness of employees in Enterprises
Promote enterprises to save energy, recycle waste, reduce environmental liability accidents and reduce operating costs
Improving the level of environmental management in Enterprises
3. Necessary Conditions and List of Information
All kinds of production, trade and service-oriented enterprises registered in the People's Republic of China may apply for certification if they meet the following relevant conditions.
1. Business License
2. Effective certification of qualifications
3. Brief Introduction of Enterprises
4. Organization chart
5. Product process flow chart
6. Planning of plant area
7. Environmental Impact Assessment Data
QC080000 Hazardous Substance Management System Standard
There are many requirements in the current or pending regulations that require the elimination of a defined set of hazardous substances, including Pb, Hg, Cd, Cr6+, PBB, and PPBE contained in electrical and electronic products.However, various regulations have different control requirements for hazardous substances,Customer requirements for hazardous substances are also different.To solve this problem in a unified way, it is necessary to have an authoritative standard issue, So that all interested parties have a unified and clear guidelines to follow, so as to achieve international technical barriers to trade in goods is minimized. In order to solve the standardization problem of hazardous substances, IEC commissioned IECQ to develop a special hazardous substance process management(HSPM) --Electrical and Electronic Components and Products Hazardous Substance Free Standard and Requirements（EIA/ECCB-954）.And developed special rules of procedureHazardous Substance Process Management Requirements（QC001002-5）for the certification of this process management systemthus providing an authoritative choice for hazardous substance management and certification.
2, The benefits of certification
1. Implement effective control over hazardous substances to meet European hazardous substances requirements and reduce corporate risks;
2. The product has obtained an environmentally friendly pass for smooth transactions worldwide;
3. Compliance with hazardous substance management of products can be guaranteed with less inspection and management costs;
4. Integration of quality and hazardous substance management systems to reduce management costs and improve efficiency;
5. Enhance long-term relationships with customers;
6. Establish a green supply chain and achieve green procurement to reduce the risk of hazardous substances due to purchased products;
7. Continuous and stable process management and product quality will be released to the world through the “IECQ Online Certificate Database” to expand the potential market;
8. Enhance the competitiveness of the organization's market
3. Prerequisites and information list
Prerequisites
1. Applicable to manufacturers, suppliers, repairers, maintainers, etc. involving electrical and electronic products.
2. The system operates for not less than 3 months
Information
Contract
2. The application form, business license and organization code certificate (confirmed within the validity period)
3. Other valid qualification certificates (product production license, etc., if applicable)
4. Company Profile
5. Organization chart
6. ISO9001 certificate or other system certification (if any);
ISO 13485: 2016
ISO 13485 the International Quality Management Systems for the design and manufacture of medical devices.
HELPS YOU WITH
Quality Control, Risk Management, Legal Compliance, Traceability and Recall, Process Improvement, Product Improvement, Operational Efficiency
The standard contains specific requirements for manufacture, installation and servicing and calls for:
Implementation of a Quality Management System with several enhancements
Risk Management approach to product development and product realisation
Validation of processes
Compliance with statutory and regulatory requirements
Effective product traceability and recall systems.
ISO 13485 contains requirements that are essential for any organization operating at any tier in the medical device and pharmaceutical supply chain.
It is especially relevant to manufacturers that wish to demonstrate applicable regulatory requirements, and by organizations whose services support medical device manufacturers.
The benefits of IS13485:
Customer satisfaction – through delivery of products that consistently meet customer requirements as well as quality, safety and legal requirements
Reduced operating costs – through continual improvement of processes and resulting operational efficiencies
Improved stakeholder relationships – including staff, customers and suppliers
Legal compliance – by understanding how statutory and regulatory requirements impact the organization and its customers
Improved risk management – through greater consistency and traceability of products and use of risk management techniques
Proven business credentials – through independent verification against recognised standards
Ability to win more business – particularly where procurement specifications require certification as a condition to supply in a highly regulated sector.
The Standardization Organization (ISO) developed the "ISO22716:2007" standard in November 2007: Cosmetics-Good Manufacturing Practices. This standard provides cosmetic manufacturers with operational guidelines for production, control, storage, and more. The ISO22716 Cosmetic International Standard regulates the management requirements of cosmetics manufacturers; hardware requirements (factory, production site, equipment, etc.), procurement and use of materials, and hygiene and quality control of product manufacturing processes, personnel hygiene management, product inspection, and abnormal quality. Disposal and product complaints and recalls.
Helps you with
Ensure product safety
Improve product quality
Help products enter the international market
Proven business credentials
GMPC (Good Manufacturing PracticeCosmetics) was first promulgated by the US Congress in 1963 to regulate pharmaceutical production. It is also the world's first GMP. The FDA, the US Food and Drug Administration, enacted food GMP in 1980 to regulate food production. In 1992, the FDA issued the Cosmetics GMP Guidelines，to guide cosmetic manufacturers. In order to ensure that the cosmetics produced and sold in its territory (including imported from outside the EU) will not cause harm to consumers' health, the European Union issued the Cosmetics Directive 76/768/EE on July 26, 1976, 2 The seventh edition of the directive was issued on the 27th of the month, and the latest directive requires factories that produce cosmetics to meet good operating practices.
Helps you with
Ensure product safety
Improve product quality
Help products enter the international market
Proven business credentials
ISO45001 is a new occupational health and safety management system standard used by ISO International Standardization Organization to replace OHSAS 18001. The release of ISO 45001 in March 2018 marks an important step in improving occupational health and safety standards worldwide. This new standard is used to help organizations around the world ensure the health and safety of their workers.
An important reason for the emergence of occupational health and safety management system is the need of world economic globalization and international trade development. The basic principle of WTO is "fair competition", which includes environmental and occupational health and safety issues.
Occupational health and safety management system is a management system standard applicable to any organization. The purpose is to reduce and prevent the loss of life, property and time caused by accidents through management.
The construction of ISO 45001 is based on the existing norms of OHSAS 18001. Its main objective is the same, which is to improve the occupational health and safety performance of the organization. At the same time, there are the following differences:
1. Using the advanced structure of ISO management system
2. Pay more attention to the "organizational environment"
3. Emphasize the responsibilities and leadership of top managers
4. Focus more on management responsibilities
5. Emphasis on risk-based thinking
6. Pay more attention to performance monitoring and measurement
2. Benefits from certification
1. Improve the viability of enterprises through risk prevention, innovation and continuous improvement;
2. Enhancing the implementation of occupational health and safety regulations and systems in enterprises;
3. Improving the level of occupational health and safety management in enterprises;
4. Help to eliminate trade barriers;
5. To produce direct and indirect economic benefits to enterprises;
6. Set up the good quality and image of the enterprise, and show the sense of responsibility of the enterprise.
3. Necessary Conditions and List of Information
All kinds of production, trade and service-oriented enterprises registered in the People's Republic of China may apply for certification if they meet the following relevant conditions.
1. Business License
2. Effective certification of qualifications
3. Brief Introduction of Enterprises
4. Organization chart
5. Product process flow chart
6. Planning of plant area
7. Occupational Health and Safety Information
ISO 14001 is the code name of environmental management system certification. ISO 14000 series standards are environmental management system standards formulated by International Organization for Standardization. It is formulated to meet the needs of international environmental protection and to meet the needs of international economic and trade development, aiming at the increasingly serious global environmental pollution and ecological destruction, ozone layer destruction, global warming, the loss of biodiversity and other major environmental problems that threaten human survival and development in the future.
Implementing ISO14001 standard in enterprises is the need of saving energy, reducing consumption, turning waste into treasure, reducing environmental expenditure and reducing cost. Through the establishment and implementation of environmental management system, it can reduce the generation and discharge of pollutants, promote waste recycling, save energy, save raw materials, avoid fines and sewage charges, and reduce costs.
2. Benefits from certification
Establishing the image of the enterprise and enhancing its popularity
Promoting enterprises to consciously abide by environmental laws and regulations
Promote enterprises to consider their impact on the environment in their production, operation, service and other activities and reduce environmental load
Enabling enterprises to obtain "green passes" to enter the international market
Enhancing the environmental awareness of employees in Enterprises
Promote enterprises to save energy, recycle waste, reduce environmental liability accidents and reduce operating costs
Improving the level of environmental management in Enterprises
3. Necessary Conditions and List of Information
All kinds of production, trade and service-oriented enterprises registered in the People's Republic of China may apply for certification if they meet the following relevant conditions.
1. Business License
2. Effective certification of qualifications
3. Brief Introduction of Enterprises
4. Organization chart
5. Product process flow chart
6. Planning of plant area
7. Environmental Impact Assessment Data
There are many requirements in the current or pending regulations that require the elimination of a defined set of hazardous substances, including Pb, Hg, Cd, Cr6+, PBB, and PPBE contained in electrical and electronic products.However, various regulations have different control requirements for hazardous substances,Customer requirements for hazardous substances are also different.To solve this problem in a unified way, it is necessary to have an authoritative standard issue, So that all interested parties have a unified and clear guidelines to follow, so as to achieve international technical barriers to trade in goods is minimized. In order to solve the standardization problem of hazardous substances, IEC commissioned IECQ to develop a special hazardous substance process management(HSPM) --Electrical and Electronic Components and Products Hazardous Substance Free Standard and Requirements（EIA/ECCB-954）.And developed special rules of procedureHazardous Substance Process Management Requirements（QC001002-5）for the certification of this process management systemthus providing an authoritative choice for hazardous substance management and certification.
2, The benefits of certification
1. Implement effective control over hazardous substances to meet European hazardous substances requirements and reduce corporate risks;
2. The product has obtained an environmentally friendly pass for smooth transactions worldwide;
3. Compliance with hazardous substance management of products can be guaranteed with less inspection and management costs;
4. Integration of quality and hazardous substance management systems to reduce management costs and improve efficiency;
5. Enhance long-term relationships with customers;
6. Establish a green supply chain and achieve green procurement to reduce the risk of hazardous substances due to purchased products;
7. Continuous and stable process management and product quality will be released to the world through the “IECQ Online Certificate Database” to expand the potential market;
8. Enhance the competitiveness of the organization's market
3. Prerequisites and information list
Prerequisites
1. Applicable to manufacturers, suppliers, repairers, maintainers, etc. involving electrical and electronic products.
2. The system operates for not less than 3 months
Information
Contract
2. The application form, business license and organization code certificate (confirmed within the validity period)
3. Other valid qualification certificates (product production license, etc., if applicable)
4. Company Profile
5. Organization chart
6. ISO9001 certificate or other system certification (if any);
ISO 13485 the International Quality Management Systems for the design and manufacture of medical devices.
HELPS YOU WITH
Quality Control, Risk Management, Legal Compliance, Traceability and Recall, Process Improvement, Product Improvement, Operational Efficiency
The standard contains specific requirements for manufacture, installation and servicing and calls for:
Implementation of a Quality Management System with several enhancements
Risk Management approach to product development and product realisation
Validation of processes
Compliance with statutory and regulatory requirements
Effective product traceability and recall systems.
ISO 13485 contains requirements that are essential for any organization operating at any tier in the medical device and pharmaceutical supply chain.
It is especially relevant to manufacturers that wish to demonstrate applicable regulatory requirements, and by organizations whose services support medical device manufacturers.
The benefits of IS13485:
Customer satisfaction – through delivery of products that consistently meet customer requirements as well as quality, safety and legal requirements
Reduced operating costs – through continual improvement of processes and resulting operational efficiencies
Improved stakeholder relationships – including staff, customers and suppliers
Legal compliance – by understanding how statutory and regulatory requirements impact the organization and its customers
Improved risk management – through greater consistency and traceability of products and use of risk management techniques
Proven business credentials – through independent verification against recognised standards
Ability to win more business – particularly where procurement specifications require certification as a condition to supply in a highly regulated sector.
Benefits of ISO9001 to your business
ISO 9001 aims to provide a practical and workable Quality Management System for improving and monitoring all areas of your business.
Achieving the ISO 9001 standard is not about establishing a set of procedures that are complicated and difficult to manage. The aim is to provide a workable management system that is suitable for your organisation. With the right support and the knowledge of your employees, you will end up with a system that will improve all areas of your organisation.
Implementing an effective and robust ISO 9001 Quality Management System (QMS) will help you to focus on the important areas of your business and improve efficiency. The management processes that are established throughout your business will provide a sound foundation, leading to increased productivity and profit. This in turn will improve your customer acquisition and retention.
Some of the main benefits of ISO 9001 certification include:
Suitable for both small and large organisations
Better internal management
Less wastage
Increase in efficiency, productivity and profit
Improved customer retention and acquisition
Consistent outcomes, measured and monitored
Globally recognised standard
Compatible with other ISO standards
A valid ISO 9001 certificate will be a prerequisite for some of your customers and a “nice to have” for others, when they are considering suppliers. It gives your customers confidence that you are working to standards and procedures that will provide them with a high standard of customer service.
Benefits of ISO 9001 to your customers
The ISO9001 standard is recognised worldwide and your customers will understand the benefits of working with companies that are ISO 9001 certified. In fact, some of your customers will only do business with certified companies because it gives them assurance that you management systems are constantly assessed and approved.
They will know from experience that working with ISO9001 certified companies provides many advantages:
Minimises mistakes
Improves reporting and communications
Better quality products and service
More reliable production scheduling and delivery
Standards maintained by annual assessments
