The company has a comprehensive ISO quality system and has formulated a series of complete quality management systems and system documents, which comprehensively cover every aspect of the product lifecycle from design, research and development, release, sales, integration, implementation, testing, acceptance, and maintenance, ensuring comprehensive control over product quality. This forms a complete closed-loop quality management system, effectively enhancing quality management efficiency. A rigorous quality monitoring mechanism has been established, through regular quality inspections, process control, quality audits, and other means, to promptly identify and resolve quality issues, continuously improving and enhancing the effectiveness and adaptability of the quality management system.

Wellthinic has accumulated implementation experience in building lighthouse projects for various industries and clients. During project execution, we provide customers with localized operation and maintenance team support, year-round uninterrupted services, and other enhanced service guarantees. Adhering to the concept of service supremacy and efficiency first, we continuously create value for customers, realize digital and intelligent reforms for enterprises, and contribute to China's smart manufacturing.

Professionalism: Capable of meeting 90% of business processes in the process industry, and realizing business differences through modular configuration.

Scalability: The completely separated development mode of front-end and back-end makes it easier to expand front-end pages and back-end logic, while supporting the reuse and expansion of existing functions.

Support for Multiple Databases: The backend encapsulates universal interfaces that can be directly called to implement common business functions, eliminating the need for developing frontend-encapsulated universal components. Page displays can be achieved simply by assembling and passing parameters.

Address and optimize the requirements for globally unified GMP compliance and standardize globally unified production processes. Ensure that the entire production process is traceable, recordable, and controllable. Strengthen compliance with the "two laws" and "two regulations" to enhance the consistency of drug quality. Maintain high standards for process safety, audit trails, and electronic records during production and testing, and reduce manual intervention to improve quality stability through increased intelligence.

Address and optimize the requirements for globally unified GMP compliance and standardize globally unified production processes. Ensure that the entire production process is traceable, recordable, and controllable. Strengthen compliance with the "two laws" and "two regulations" to enhance the consistency of drug quality. Maintain high standards for process safety, audit trails, and electronic records during production and testing, and reduce manual intervention to improve quality stability through increased intelligence.