Complete Product Listing

Shanghai Trifecta Pharma Co. Ltd offers one of the broadest portfolios of active pharmaceutical ingredients (API)—the ingredients responsible for the therapeutic effects of different medicines—to more than 40 countries.

Quality begins at step one. Shanghai Trifecta Pharma Co. Ltd uses an established testing and verification process to ensure the suitability of active ingredients sold to our cliental.

“Active pharmaceutical ingredients (APIs) are at the very heart of modern medicine, and form the basis for much of the effective and innovative treatments in place and under development.”

APIs are regulated by some of the most rigorous and stringent legislation ever passed. Compliance with these regulations and with best industrial, clinical and manufacturing practices is an absolute necessity for any actor in the pharmaceutical products supply chain. Quality assurance, clinical trials and in-use assessment are all key parameters for the various stakeholders to review.

Shanghai Trifecta Pharma Co. Ltd has a team in place inspecting and regulating our sources to ensure the highest quality active pharmaceutical ingredients are being supplied to our cliental.

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
Not only do we supply the product and exceptional customer service we also provide a full Drug Master File and supporting documentation.

Drug Master File (CTD Format and others)
GMP Certificate
Other Required Documentation

Shanghai Trifecta Pharma Co. Ltd supports our cliental from start to finish and has developed strategic partnerships in South America, Europe, Asia, North America, Africa and the Middle East based on mutual cooperation and mutual benefit.