Contract Development and Manufacturing Organization (CDMO)

Category: *CDMO

Booth No: M520

Characteristic

Your strategic partner for success
 From R&D process development to process validation
 From pre-IND scale to commercial scale
 From chemical sourcing to CMC documentation
 From drug substance to drug product
 PICS/GDP services for labelling, packaging, and logistics
All GMP-compliant

As a contract development and manufacturing organization (CDMO), Formosa Laboratories offers full-service for both general and high potency API (HPAPI) for all stages of drug development for both clinical trial material) and commercializedproducts. Our GMP compliance has been approved by TFDA, US FDA, BGV of Germany, EDQM and PMDA 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 as well as formulation development to FDF filling for both liquid and lyophilized drug products.

With the fully-integrated R&D and manufacturing capabilities from API to FDF, Formosa is able to provide one-stop-shop CDMO services delivering our client drug product.