The cGMP pilot plant facility is built as per international guidelines to meet both domestic and international regulatory requirements.

Has the ability to manufacture clinical materials, small volumes for marketing and for stability studies.

The plant is equipped with a 19 liter Fermentor, a Lyophilizer, and downstream processing equipment for purification, formulation and filling including PFS (Pre Filled Syringe).

The PFS filling room facility received GMP certification to satisfy schedule M requirements. It also received the WHO GMP Certification.