Close
Novotech
Jabsco PureFlo 21 Single Use

WuXi STA’s new drug product manufacturing facility passes first European MPA GMP Inspection

Note* - All images used are for editorial and illustrative purposes only and may not originate from the original news provider or associated company.

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

– Access the Media Pack Now

– Book a Conference Call

Leave Message for Us to Get Back

Related stories

Novo Nordisk OpenAI Partnership Accelerates Drug Development

Danish pharmaceutical major Novo Nordisk has entered into a...

Smart Sensors Elevating Pharma Process Control Systems

The deployment of intelligent sensing technology is fundamentally reshaping how pharmaceutical manufacturers manage complex production environments. By providing granular, real-time data at critical control points, these advanced instruments allow for instantaneous process adjustments, ensuring that every batch meets the most rigorous standards of quality and safety.

Next Gen Filtration Systems for Pharma Facilities

The evolution of filtration technology is playing a critical role in enhancing the safety and efficiency of pharmaceutical manufacturing. Next-generation filtration systems—featuring advanced membrane materials, automated integrity testing, and single-use designs—provide superior contamination control and operational agility, ensuring that modern drug products meet the most stringent sterility and purity requirements.
- Advertisement -

STA Pharmaceutical Co., Ltd., (WuXi STA) – a subsidiary of WuXi AppTec – announces that its new drug product manufacturing facility in Waigaoqiao Free Trade Zone of Shanghai has passed its first GMP inspection by the European Medical Products Agency (MPA).

The new facility was opened at the end of 2018, and the successful inspection demonstrates the outstanding quality control system and rapid development of WuXi STA’s drug product services.

In 2017, WuXi STA merged with WuXi AppTec’s Pharmaceutical Development Services unit, realizing a seamless integration of chemistry, manufacturing and control (CMC) services. Two new commercial drug product facilities – in Shanghai and Wuxi City – have come into operation, enabling WuXi STA to support solid dosage drug development from preclinical to commercial, with several phase III and commercial drug product projects underway.

WuXi STA has received FDA inspections at both its API and advanced intermediate manufacturing facility in Jinshan (Shanghai), and API R&D & manufacturing facility in Changzhou. As a leading global Contract Development and Manufacturing Organization (CDMO), WuXi STA has successfully passed inspections by regulatory bodies in the U.S., Canada, EU, Switzerland, China, Australia and New Zealand to supply APIs and GMP advanced intermediates for partners.

“We are very proud to have passed the European MPA GMP inspection,” commented Ms. Mei Hao, Vice President of Quality at WuXi STA. “We will continue to strengthen our global quality control system to meet the most stringent regulatory requirements and ensure the quality of services to our partners worldwide. It is a key milestone in our efforts to build geographically integrated capabilities for both drug product and substance development and manufacturing.”

“Quality is not just a core competency, it is ingrained throughout our culture at WuXi STA. The new facility passing the MPA’s GMP inspection is further proof of our commitment to the highest possible quality standards. We look forward to empowering more customers to develop innovative drugs faster and more efficiently for the benefit of patients around the world,” said Dr. Minzhang Chen, CEO of WuXi STA.

About WuXi STA
STA Pharmaceutical Co., Ltd., a subsidiary of WuXi AppTec (WuXi STA), is a leading pharmaceutical development and manufacturing capability and technology platform company serving the life sciences industry, with operations in China and the United States. As a premier Contract Development and Manufacturing Organization (CDMO), WuXi STA offers our worldwide partners efficient, flexible and high-quality solutions for Active Pharmaceutical Ingredients (APIs) and finished dosage forms. For more information, please visit: http://www.STApharma.com

About WuXi AppTec
WuXi AppTec is a leading global pharmaceutical and medical device open-access capability and technology platform company with global operations. As an innovation-driven and customer-focused company, WuXi AppTec provides a broad and integrated portfolio of services to help our worldwide customers and partners shorten the discovery and development time and lower the cost of drug and medical device R&D through cost-effective and efficient solutions. With its industry-leading capabilities such as small molecule R&D and manufacturing, cell therapy and gene therapy R&D and manufacturing, and medical device testing, WuXi platform is enabling nearly 3,500 innovative collaborators from more than 30 countries to bring innovative healthcare products to patients, and to fulfill WuXi’s dream that “every drug can be made and every disease can be treated.” Please visit: http://www.wuxiapptec.com

Latest stories

Related stories

Novo Nordisk OpenAI Partnership Accelerates Drug Development

Danish pharmaceutical major Novo Nordisk has entered into a...

Smart Sensors Elevating Pharma Process Control Systems

The deployment of intelligent sensing technology is fundamentally reshaping how pharmaceutical manufacturers manage complex production environments. By providing granular, real-time data at critical control points, these advanced instruments allow for instantaneous process adjustments, ensuring that every batch meets the most rigorous standards of quality and safety.

Next Gen Filtration Systems for Pharma Facilities

The evolution of filtration technology is playing a critical role in enhancing the safety and efficiency of pharmaceutical manufacturing. Next-generation filtration systems—featuring advanced membrane materials, automated integrity testing, and single-use designs—provide superior contamination control and operational agility, ensuring that modern drug products meet the most stringent sterility and purity requirements.

Real Time Data Analytics in Pharma Utility Systems

The integration of real-time data analytics is revolutionizing the management of pharmaceutical utility systems, providing facility managers with actionable insights into the performance of critical infrastructure. By transforming raw sensor data into meaningful intelligence, manufacturers can optimize energy use, prevent equipment failures, and ensure that utilities like HVAC and water always operate within validated parameters for high-quality drug production.

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

– Access theMedia Pack Now

– Book a Conference Call

Leave Message for Us to Get Back

Translate »