Formosa Laboratories, Inc. commits itself to the manufacture of all its pharmaceutical products in accordance with the current Good Manufacturing Practices (ICH Q7A) and by the methods described in specific drug master files or equivalent documents.

We have been audited by DOH of Taiwan, , the US FDA, BSG of Germany, PMDA of Japan, and a number of local and foreign companies. Any duly authorized individual is invited to inspect our facilities at any reasonable time with pre-notification.

We are also ISO 9001 - certified.