Qualence Life Sciences, as a renowned Manufacturer and Exporter of Pharmaceutical Products, upholds high quality standards in order to satisfy customers worldwide. We implement our quality policy through our Quality Management System based on current Good Manufacturing Practices (GMP & cGMP) in accordance with national and international regulatory standards like WHO, FDA, etc.international regulatory standards such as WHO, FDA, etc. With constant product monitoring, we conduct all of our manufacturing activities in an automated & controlled environment.

Our Quality Assurance (QA) services include exemplary environmental monitoring, calibration and validation programs, from raw material procurement to final delivery. Standard Operating Procedures (SOPs) have been established to guide the way in which each of the activities that are performed in the plants and laboratories is to be carried out. The department coordinates the work of the design, development and manufacturing teams, as well as maintaining the quality management system throughout the organization.

We have established Quality Control (QC) Laboratories with separate areas for testing raw materials, testing instruments, testing microbiology, testing sterility and testing packaging. In our laboratories, we have sophisticated equipment such as Dissolution testers, UV-Visible spectrophotometers, HPLCs, GLCs, FTIRs, Atomic Absorptions, and other test instruments in accordance with GLP and ISO 9001 guidelines. Having a strong quality control department and knowing that our analytical results are accurate and consistent is the key to our success.