The lab is a cGMP facility and approved by both HPFBI and FDA; all analytical equipment are fully qualified, all stability chambers are mapped and maintained within ICH and VICH guideline conditions. Our quality systems ensure that we are constantly in a state of compliance. Our analytical laboratory covers over 5,000 sq. ft.
TetraGenx’s GMP facility (1,500 sq ft.) is supported by staff with 30 years of pharmaceutical development, quality assurance, analytical services, packaging, turn-key clinical supply and commercial manufacturing experience.
Covering 4,600 sq. ft., our development facility is fully equipped to develop your products. Any product development needs you may have, we will be able to answer with the equipment found in this facility.