Brilliant’s Good Laboratory Practice (GLP) certified Quality Control Department features laboratories for Instrumentation, QC & Analytics, Chemical Analysis, and Microbiology. It is equipped with an array of sophisticated analytical equipment for testing of vaccines - from raw materials to finished products and all intermediates, to ensure the quality of materials at every stage of manufacturing.

Animal Testing Facilities

• Capacity to hold multiple species of laboratory animals to test in-process and finished goods
• Designed based on uni-directional flow to clearly segregate clean and unclean activities
• Bio-safety level compliant facility for large animal testing with in-built lab facility
• PM & Effluent treatment rooms
• Separate rooms to house groups of animals
• QC team offering includes ICH stability testing

Quality Assurance

Brilliant Bio Pharma adheres to a well laid down ‘Quality Policy’ and is committed to comply with the requirements of Quality Management Systems accredited by ISO 9001:2015 while continually improving its effectiveness. The objective of the QA Department is achieved by implementing current code of Good Manufacturing Practice as per national and international guidelines. The Department ensures adherence to the well-designed protocols at every stage of production and testing by assuring end-to-end consistency from raw material inward to finished product dispatch.