Powered by an intelligent engine, the system integrates real-time data feedback to efficiently manage the full-process handling of samples. Through parallel computing and dynamic optimization, it enables unattended operation and enhances the level of automation.

The system features built-in barcode scanning and image recognition, which automatically verify and track samples throughout the entire process. Key data is stored in real-time in a high-performance database to create detailed records. The software automatically generates compliant audit reports, ensuring data integrity and mitigating the risks of sample confusion and loss.

The system utilizes a microservices architecture, with each module operating independently to ensure flexibility and scalability. Standardized API interfaces facilitate seamless integration of new modules. Combined with containerized deployment, the system can rapidly adapt to a variety of scenarios. It operates efficiently across a wide range of throughput levels, from low to high, ensuring a strong return on investment.

With a high-definition touch screen and a responsive interface, the operation is intuitive and smooth. RBAC ensures security. Remote monitoring allows real-time mastery of the device and sample status. The intelligent engine analyzes data through AI algorithms and provides predictive maintenance and optimization suggestions to ensure the efficient operation of the device.

Independently developed latex particles with uniform nanoscale particle size, diverse chemical surfaces, and low refractive index, which have good stability, do not settle, and have high sensitivity. They are standard particles measured and recommended by the international AIST and NIST.

Develop a highly active and highly stable enzymatic reaction system with good substrate specificity and stable color development to ensure the accuracy and reliability of biochemistry tests.

With fine process management and strict quality control, there is an excellent batch-to-batch difference of tests, meeting the high standards required for clinical diagnosis.

It has passed the ISO 9001 and ISO 13485 quality system certifications, and obtained the ISO/IEC 17025 laboratory accreditation certificate frequently issued by CNAS. It realizes the traceability of the quantity values of all products in the product line, providing a solid guarantee for product quality.

Using genetic engineering methods, produce high-quality recombinant proteins in expression systems such as Escherichia coli, yeast, and mammalian cells, and apply them to the fields of diagnosis and vaccines.

A complete technical system for monoclonal antibody preparation, covering the entire process from antigen design, immunization, cell fusion to clone screening and large-scale culture.

Develop highly active and highly specific enzymatic tests and apply them to fields such as biochemistry analysis and molecular diagnosis to improve detection performance.

Establish a strict quality control system for bioactive materials to ensure the purity, activity, and batch consistency of bioactive materials, providing a guarantee for the quality of downstream products.

The world's first highly efficient protein expression system, which realizes the efficient and high-quality expression of complex proteins and provides key technical support for vaccine research and development.

Virus-like particle (VLP) technology, which mimics the virus structure but does not contain viral nucleic acid, has high safety and good immunogenicity, and is an important direction for modern vaccine development.

Develop innovative adjuvant formulations to enhance the immune response of vaccines, improve the protection effect, and extend the protection time.

The technology for developing multivalent vaccines integrating multiple antigens, which can prevent multiple diseases with a single vaccination, improving the convenience and coverage of vaccination.