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As a contract development and manufacturing organization (CDMO), Ely Biotech offers full-service for both general and high potency API (HPAPI) for all stages of drug development for both clinical trial material (CTM) and commercialized (NDA). Our GMP compliance has been approved by DOH of Taiwan, US FDA, BGV of Germany, EDQM and PMDA of Japan since 2000.

Process development and route optimization are core competencies of our business. The company has a dedicated staff of professional process chemists and engineers with significant experience and expertise in the development of robust cGMP chemical processes.


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