Manufacturing Facilities
Etana has built a high-end biopharmaceutical manufacturing facility with a gross floor area of 6,400 sq.m. The Plant construction of Etana was designed by the world class consultant – NNE Pharmaplan – to meet the standard of cGMP, PIC/S and EU GMP for its design concept.
The factory has already passed GMP audits by an Indonesian National Agency of Drug and Food Control (BPOM) and received GMP Certification in December 2019. They are equipped with world-class technology of laboratory instrument, pharmaceutical water systems, clean room HVAC systems, utility systems, environment monitoring systems, and other equipments & facilities.
Our manufacturing process and facilities are strictly controlled through cGMP guideline that comply with global regulatory requirement. Our standard is already complied with cGMP, PIC/S, and EU GMP with the purposes to cater to overseas and domestic markets.
Our facilities have the capability to produce biosimilar/biology sterile solutions with packaging of injectable in Prefilled Syringe (PFS), and in planning for facility of injectable in vials & cartridge.
