GreatLight Supplier Code Of Conduct

Suppliers must comply with all applicable laws and regulations of the countries, regions, and localities in which they operate.

Prohibition of forced labor and child labor.

Provision of fair working conditions and compensation.

Non-discrimination and respect for freedom of association.

Working hours must comply with local legal requirements. Employees’ weekly working hours should not exceed the legal maximum, ensuring adequate rest periods.

Suppliers shall provide a safe and healthy working environment for their employees, taking proactive preventative measures to control occupational hazards and prevent work-related injuries and illnesses.

Suppliers must obtain all necessary environmental permits, approvals, and registrations, and comply with their terms.

Commit to improving the efficiency of energy and resource use.

Implement effective measures to reduce and control pollutant emissions to air, water, and land.

Manage waste, especially hazardous waste, safely and responsibly.

Prohibit all forms of corruption, extortion, embezzlement, and bribery. Suppliers must not offer any form of bribe or undue advantage to GreatLight employees or their relatives to gain improper benefits.

All business activities shall be accurately and fairly recorded in books and records.

Comply with all applicable anti-trust and fair competition laws.

Respect and protect intellectual property rights.

We support initiatives to ensure supply chains are free from conflict minerals and modern slavery, and expect suppliers to conduct due diligence in these areas.

We encourage Suppliers to establish effective management systems to drive continuous compliance and improvement with the requirements of this Code.

reserves the right to monitor Suppliers’ compliance with this Code through assessments and audits (announced or unannounced). Any serious violation of this Code may lead to the termination of the business relationship.

ISO 9001 is defined as the internationally recognized standard for Quality Management Systems (QMS). It is by far the most mature quality framework in the world. More than 1 million certificates were issued to organizations in 178 countries. ISO 9001 sets standards not only for the quality management system, but also for the overall management system. It helps organizations achieve success by improving customer satisfaction, employee motivation, and continuous improvement. * The ISO certificate is issued in the name of FS.com LIMITED and applied to all the products sold on FS website.

IATF 16949 is an internationally recognized Quality Management System (QMS) standard specifically for the automotive industry and engine hardware parts production quality management system certification. It is based on ISO 9001 and adds specific requirements related to the production and service of automotive and engine hardware parts. Its goal is to improve quality, streamline processes, and reduce variation and waste in the automotive and engine hardware parts supply chain.

ISO/IEC 27001 is an international standard for managing and processing information security. This standard is jointly developed by the International Organization for Standardization (ISO) and the International Electrotechnical Commission (IEC). It sets out requirements for establishing, implementing, maintaining, and continually improving an information security management system (ISMS). Ensuring the confidentiality, integrity, and availability of organizational information assets, obtaining an ISO 27001 certificate means that the enterprise has passed the audit conducted by a certification body, proving that its information security management system has met the requirements of the international standard.

ISO 13485 is an internationally recognized standard for Quality Management Systems (QMS) specifically tailored for the medical device industry. It outlines the requirements for organizations involved in the design, development, production, installation, and servicing of medical devices, ensuring they consistently meet regulatory requirements and customer needs. Essentially, it's a framework for medical device companies to build and maintain robust QMS processes, ultimately enhancing patient safety and device quality.