SOLUTIONS

Design and 

Design a plant layout that meets GMP standards for pharmaceutical companies, including reasonable planning of production areas, storage areas, quality control areas, etc., to ensure the efficient flow of materials and personnel. For example, place the filling workshop with high cleanliness requirements on the upwind side to reduce pollution.

Equipment Supply and Integration

Provide one-stop supply from API production equipment to preparation filling and packaging equipment, such as efficient reactors, advanced isolator filling machines, etc., and integrate and optimize them to ensure the coordination of various equipment.

Process

Develop appropriate processes for different types of drugs, such as optimizing the synthesis route of chemical synthetic drugs, determining the fermentation and purification process of biological drugs, and improving the quality and output of drugs.

Quality

Establish a complete quality control system, from raw material testing, production process monitoring to finished product inspection, and use advanced testing instruments and methods, such as high-performance liquid chromatography, to ensure stable and reliable drug quality.

Project Implementation and Verification

Responsible for the construction of the entire project, and verify the equipment and process to ensure that the system meets the design requirements and regulatory standards, and ensure smooth production.

Training and

Provide operation training and technical support for pharmaceutical company employees, and respond to equipment maintenance, process improvement and other needs in a timely manner during the after-sales stage to ensure continuous production.