WuXi STA Expands Capabilities at Changzhou Campus

WuXi STA has added two reactors at its Changzhou campus in China, enhancing capacity and capability at its TIDES contract research, development and manufacturing platform for oligonucleotide, peptide and related synthetic conjugates. The reactors have capacity of 2,000 liters each, taking total volume for solid-phase peptide synthesizers to more than 10,000 liters.

The company has also added a new twin-column continuous purification system that can handle kilogram-scale peptides and oligonucleotides. WuXi STA said the continuous process enables a faster turnaround time and lower solvent consumption, allowing for more efficient and sustainable manufacturing.

CEO Minzhang Chen commented: " We are committed to continuously enhancing our WuXi TIDES CRDMO platform's capacity and capability to expedite the development and commercialization of more innovative therapies for patients worldwide."

In January, the company announced that its first drug product continuous manufacturing line for oral solids went into operation at its site in Wuxi City, China. Wuxi STA said the new line provides customers “an enhanced oral drug development solution that enables higher yields and a shorter time to market.

Author: Elaine Burridge, Freelance Journalist

© WuXi STA
© WuXi STA

Innovation Pitch

The Start-up Platform for Chemistry & Life Sciences
Discover Tomorrow’s Innovators

The Start-up Platform for Chemistry & Life Sciences

CHEManager Innovation Pitch supports innovation in the chemistry and life sciences start-up scene. The platform allows founders, young entrepreneurs, and start-ups to present their companies to the industry.

Whitepaper

Excellence in Pharmaceutical Distribution and The Critical Role of Good Distribution Practice (GDP)
Setting the Standard

Excellence in Pharmaceutical Distribution and The Critical Role of Good Distribution Practice (GDP)

Are you ready to elevate your pharmaceutical operations? Download our exclusive whitepaper and discover how compliance with Good Distribution Practice (GDP) is essential for the safety and integrity of pharmaceuticals.