Claris’ manufacturing facilities are designed to produce aqueous and oil-based products in glass/PE containers and bags. The facilities practice cGMP and are ISO 9001:2000 certified. Apart from manufacturing for Claris, these facilities also cater to the needs of companies in India and abroad for international markets on contract manufacturing.

International regulatory authorities including USFDA, MHRA (UK), TGA (Australia), NAM(Finland), GCC (Gulf Co-operation Council including Saudi Arabia, U.A.E. and other Middle East countries), ANVISA (Brazil) and INVIMA (Colombia) have approved the sterile parenteral preparation manufacturing facilities.  

The company has capabilities in bringing laboratory batches to full production scale successfully, through its process engineering competence. This technological excellence also goes beyond process and it has executed several projects with its technology platforms including: