Recently, the provincial laboratory proficiency testing project organized by Jiangsu Provincial Drug Administration and undertaken by Jiangsu Institute of Food and Drug Supervision and Inspection announced the results of the competition. The QC department of Nanjing Leecan achieved excellent results and received a "satisfactory" evaluation, which was highly recognized by the organizers and sponsors.

   A total of 191 laboratories from across the province participated in the Jiangsu Provincial Laboratory Capability Verification competition, which was extremely competitive. This validation is divided into two items: "Determination of Drug Content by High Performance Liquid Chromatography" and "Determination of Drug Content by UV Absorption Coefficient Method", and the results are judged by Z-ratio score| The smaller the Z |, the higher the accuracy. The QC department of Leecan has a | Z | of 0.02 in the project "Determination of Drug Content by High Performance Liquid Chromatography", which is the best level among all participating laboratories; In the project "Determination of Drug Content by UV Absorption Coefficient Method", | Z | is 0.51, exceeding the level of 80% of participating laboratories.

   This is the first time that Leecan has participated in the provincial-level capability verification. Chen Xi, Ou Mingyue, and Zhao Sijia, three teachers from the QC department of Leecan in Nanjing, have carefully controlled every aspect of the competition project, continuously explored method parameters, thoroughly reviewed literature and materials, meticulously debugged the testing equipment, and conducted blind inspection on September 21, 2024. The results and related materials were sent as required. Their outstanding achievements and high recognition vividly illustrate the work philosophy of the QC department of Leecan, which is "timely, accurate, rigorous, and scientific", and also demonstrate the superb inspection technology level of the QC team members.

  Leecan always adheres to the principle of data reliability, using the strictest standards and the most authentic data to make the most objective and accurate evaluation of the quality of each batch of drugs, ensuring that every link in the production and testing process goes through strict verification procedures, continuously and stably guaranteeing the quality of each batch of products, and providing the market and patients with safe, high-quality and efficient drugs that "reassure us, patients, regulators, and society".