Pharmaceutical
Product Quality
Management

Pharmaceutical Quality Standards

Maintaining GMP PIC/S Standards

Union Drug Labs. Ltd. received GMP (Good Manufacturing Practice) certification from the Food and Drug Administration (FDA) in 1990 and further obtained PIC/S (Pharmaceutical Inspection Co-operation Scheme) standards in 2015. The company is committed to producing modern medicines with high manufacturing standards, complying with laws, and strictly adhering to the requirements of drug registration. Our production processes are highly clean and safe, ensuring that our pharmaceutical products are effective and efficacious, thereby efficiently meeting consumer needs.

Selection and Verification of Every Process

Union Drug Labs. Ltd. has established a strict and rigorous quality management system for pharmaceutical products. This begins with the selection of high-quality raw materials and packaging used in drug production, extends to the design of the manufacturing facility, the drug production operations, and the quality inspection of equipment, instruments, and machinery. It also includes quality control analysis of products during the manufacturing process until they become finished pharmaceutical products. We also monitor and study the quality of all pharmaceutical products, including those released for sale to customers.

Committed to Continuous Development and Improvement

Union Drug Labs. Ltd. has always recognized the importance of feedback from both drug distributors and consumers. These processes ensure the company's quality management system maintains high standards in accordance with GMP PIC/S principles. The company is strongly committed to continuously developing, improving, and innovating new formulations using modern technology. This dedication allows us to produce high-quality medicines that effectively meet the needs of both customers and consumers.