The company operates under a comprehensive ISO quality management system, with well-defined quality management systems and documentation that fully cover every stage of the product lifecycle: design, development, release, sales, implementation, integration, testing, acceptance, and maintenance. This ensures end-to-end quality control, forms a closed-loop quality management cycle, and effectively enhances quality management efficiency.

The company has accumulated extensive experience in delivering Benchmark Projects across diverse industries and customers. During project execution, the company provides localized maintenance support and round-the-clock service during holidays, ensuring premium service assurance. Adhering to the philosophy of "Service Excellence, Efficiency Priority", Wellthinic continuously creates value for customers, enabling their digital transformation while contributing to China's Smart Manufacturing initiatives.

Covers 90% of business processes in the process industry, enables business differentiation through modular configuration

Fully separated front-end and back-end development architecture, supporting the reuse and expansion of existing functionalities

Backend-encapsulated general interfaces, direct invocation of these interfaces enables common business operations without requiring frontend development, frontend-general components allow page display through direct parameter assembly and transmission.

It is required to solve the problem of a large number of informatization systems and the contradiction between demand and supply. Currently, frequent market changes lead to increased plan modifications, resulting in inefficient resource utilization and inflexible deployment. The plant faces challenges such as numerous products, small batches, and difficulties in agile switching. Low collaboration efficiency and ineffective information flow during production can even trigger operational errors. This scenario not only incurs substantial resource costs but also suffers from poor traceability due to information silos.

It addresses and optimizes the requirements for ensuring global unified GMP compliance and the standardization of global unified process flows. All operations in the production process are traceable, recordable, and controllable. It strengthens compliance with the requirements of the "Two Laws" and "Two Regulations", thereby enhancing the consistency of drug quality. The process safety, audit trails, and electronic record standards in production and testing are relatively high. By leveraging the improvement of intelligent levels, it reduces manual intervention and enhances quality stability.