This project will coordinate the manufacturing strengths in Taiwan and increase the visibility of Taiwan's pharmaceutical capabilities. It further demonstrates the cooperation  between Japan's and Taiwan's pharmaceutical companies.

The manufactured batches will be used to further support Bioequivalence (BE) studies and then submitted to Japan's PMDA for approval. Upon PMDA's approval, Bora will be the commercial manufacturing site for the generic product production. Bora Pharmaceuticals' sites already have an excellent track record with many regulatory agencies around the world including the USFDA, MHRA, TFDA, ANVISA, Health Canada, and many others.