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Bio B2BFormosa Laboratories, Inc 〉Contract Development and Manufacturing Organization (CDMO)

Contract Development and Manufacturing Organization (CDMO)


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 process


As a contract development and manufacturing organization (CDMO), Formosa Laboratories (Formosa Labs) 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 Research 
Process development and route optimization are core competencies of our business. Formosa Labs has a dedicated staff of professional process chemists and engineers with significant experience and expertise in the development of robust cGMP chemical processes.

Analytical Support 
Formosa Labs has a dedicated and experienced analytical team providing comprehensive analytical support spanning early stage development through commercial API manufacturing. We understand the importance of timely and quality analytical support to the success of your project. Therefore, we maintain a high ratio of analytical support to chemists and engineers on a project.

Regulatory Service 
Formosa Laboratories, Inc. provides comprehensive regulatory support encompassing early stage drug substance development through commercial API manufacturing including filing support for Investigational New Drug Applications (INDs), New Drug Applications (NDAs), Abbreviated New Drug Applications (ANDAs) and Drug Master Files (DMF) as well as regulatory strategic planning.
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