Recently, two customized dissolution testers DT07TX with eight cups and 2L dissolution cups tailored by Haiyida for Jiangsu Ailande have been successfully delivered to the customer's factory. To ensure the rapid deployment of the equipment, Haiyida immediately dispatched senior engineers to the site, responsible for the installation, commissioning, and mechanical verification of the equipment throughout the process, ultimately winning customer recognition with professional and efficient services.

Dissolution testing is the "core checkpoint" in the quality control of oral solid preparations, which directly affects the safety and effectiveness of the drug. The specification accuracy of the dissolution analyzer is the key factor determining the reliability of the testing results. Due to the special requirements of the vitamin tablet research and development experiment, Jiangsu Ailande has put forward a customized requirement of 2L for the dissolution cup volume. Compared with conventional specifications, large volume dissolution cups have advantages in temperature control stability, stirring uniformity, and other aspects

Faced with higher challenges in backup performance, it has also increased the technical difficulty for this on-site service.

To ensure that the equipment meets the experimental standards, Haiyida engineers strictly follow industry standards and enterprise quality systems to carry out the full process mechanical verification work, including four core links:

Comprehensive equipment inspection: Conduct a thorough inspection of the mechanical structure, drive motor, stirring blade components, temperature control system, and various sensors of the dissolution instrument to ensure that each component is defect free, securely connected, and accurately calibrated, laying a solid foundation for the stable operation of the equipment. Simulated operation test: Based on the actual experimental scenario of the customer, multiple sets of different speed, temperature, and operating time parameters are set to simulate the operating status of the equipment under various working conditions. The response speed, parameter stability, and operating noise of the instrument are monitored and recorded in real time to verify the adaptability and reliability of the equipment.

Dissolution performance testing: Standard control samples are used for actual dissolution testing experiments. By accurately collecting dissolution data at different time points, the accuracy of the equipment's detection of drug dissolution rate and degree is analyzed to ensure that the data meets pharmacopoeia and customer research and development standards.

Data recording and analysis: Systematically record, organize, and statistically analyze all validation process data to form a complete validation report. Verify the repeatability and consistency of the instrument through data comparison, and provide reliable equipment performance basis for customers' subsequent experiments.

Since its establishment, Haiyida has always adhered to the core concept of "relying on quality and winning with efficient service", and has continued to deepen its cultivation in the field of customized equipment research and development and technical services. We are well aware that every precise dissolution instrument carries the pharmaceutical company's commitment to drug quality and is closely related to the medication safety of millions of patients.

The customized service provided to Jiangsu Ailande this time is not only a test of Haiyida's technical strength, but also a witness to customer trust. In the future, Haiyida will take this cooperation as a new starting point, continue to polish core technologies, optimize service processes, deeply cultivate the pharmaceutical quality control technology chain, and provide high-quality equipment and solutions for more pharmaceutical companies with its hardcore technological strength and thoughtful full cycle services, effectively safeguarding the defense line of drug quality and safety.