Formosa Laboratories, Inc. commits itself to the manufactures of all its pharmaceutical products in accordance with the current Good Manufacturing Practices (ICH Q7) and by the methods described in specific drug master files or equivalent documents.
We have been audited by TFDA, , US FDA, BGV of Germany, EDQM, PMDA of Japan, and a number of multinational pharmaceutical companies. Any duly authorized individual is invited to inspect our facilities at any reasonable time with pre-notification.
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