GreatLight Environmental Policy - GreatLight CNC Machining

This policy applies to all GreatLight facilities, operations, and employees in China and Singapore.

We commit to fulfilling our environmental responsibilities through the following actions:

Strictly comply with all applicable environmental laws, regulations, and other requirements, and strive to exceed these standards where feasible.

Prioritize the use of energy-efficient equipment and processes, continuously monitor and reduce energy consumption.

Implement water conservation measures and optimize the recycling of coolants in production processes to reduce freshwater consumption.

Reduce emissions of air pollutants, wastewater, and noise through source control, process optimization, and end-of-pipe treatment.

Manage chemicals used in production safely and responsibly to prevent leaks and environmental contamination.

Adhere to the principles of “Reduce, Reuse, Recycle” in waste management.

Sort and achieve 100% recycling of metal scrap (e.g., aluminum chips, steel chips).

Ensure safe disposal of hazardous waste (e.g., waste cutting fluid, waste oil) using only licensed partners.

Regularly review environmental objectives and targets, and continuously enhance environmental performance through investments in green technology and management optimization.

We are committed to monitoring and reducing our carbon footprint and greenhouse gas emissions associated with our operations.

We expect and encourage our suppliers and partners to adopt equivalent environmental standards.

Management is responsible for providing the necessary resources to ensure the effective implementation of this policy. Every employee is responsible for understanding, complying with, and contributing to the successful implementation of this policy.

This policy is publicly available and communicated to all persons working for or on behalf of GreatLight.

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.