Our Quality & Assurance department is charged with a simple mission – Ensure delivery of Zero-Defect Capsules to our customers.

 

Behind this simple mission are stringent procedures and benchmarks which govern the three stages that the raw materials pass through; pre-production, production and post-production.

 

The Q&A department is equipped with the latest testing equipments and instruments to help achieve its mission. 

 

The raw-materials and capsules undergo a continuous series of inspections which are performed in accordance with US FDA cGMP and WHO GMP standards. All our capsules are visually inspected for various defects and production processes are tightly controlled to ensure consistency of product and subsequent performance on various high-speed capsule filling machines.