Trifecta Pharma Co. Ltd, Shanghai, offers one of the broadest portfolios of active pharmaceutical ingredients (APIs) to customers in more than 40 countries. The production of APIs, the ingredients responsible for the therapeutic effects of individual medicines, is a highly regulated area and we are proud to uphold rigorous industrial, clinical and manufacturing processes with regard to APIs.

We have a dedicated team responsible for inspection and regulation of our suppliers to ensure the best quality APIs are distributed to our customers. Trifecta Pharma Co. Ltd Shanghai is committed to transparency in quality assurance, clinical trials and in-use assessment results and welcomes reviews from stakeholders.

Trifecta Pharma Co. Ltd’s customers are issues with a Drug Master File, GMP Certificate and other required documentation and can be assured that industry best practice is followed with the use of the following testing:

  • Good manufacturing practices (GMP)
  • Current good manufacturing practice (cGMP) analytical chemistry – QC release
  • Environmental monitoring in pharmaceutical production
  • Method development, optimization and validation
  • Microbiological testing
  • Particle analysis
  • Stability studies
  • Water system validation

A complete listing of Trifecta Pharma Co. Ltd. Shanghai’s APIs can be reviewed here.