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Track records on pharmaceutical fields

 Have been supplying some bulk or intermediate of
 pharmaceutical ingredients to the drug companies in
 both domestic and abroad

 Fully comply with c-GMP requirement

Have got the approval for manufacturing and supplying the intermediate (ingredient + phospholipid) of ophthalmic liposomal drug for injection from both FDA and EMEA

February 2000
EU Authority (France) Audit
March 2000

 Submit 5 kinds of DMF to both FDA and EU, and update
 every year

 Have got vendor audits from leading drug companies
 and passed their demand standards

Novartis, Abbott, Gilead, QLT, Aronex, Eisai, Yamanouchi Pharmaceutical, Taiho Pharmaceutical, etc.