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Zhejiang East Asia Pharmaceutical is a leading Chinese pharmaceutical company focused on the development and manufacture of active pharmaceutical ingredients (APIs), intermediates, and finished dosage forms. The company has multiple products approved in China and internationally. It conducts bioequivalence studies for generic drugs such as trimebutine maleate tablets and epalrestat tablets. Several products have passed cGMP certification as well as EU EDQM and Japan PMDA certifications. The company’s clinical results are primarily related to bioequivalence trials for generics.
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