Ausia


Ausia BioTech, located in Hangzhou, China, was founded in 1993 to offer comprehensive sterile manufacturing solutions and customized support services to meet specific client requirements. Ausia is a contract manufacturing organization that specializes in aseptic manufacturing of lyophilized vials. Our own in-house pharmaceutical products include an array of antibiotics.

Our vision has always been to provide high-quality, tailored manufacturing services as an outsourced partner to other pharmaceutical and health care firms. We welcome your challenges, especially if you have a product with difficult lyophilization cycle or unusual processes.

Our 400-strong team is committed to provide you professional services at all times. We might operate on large scale but we are very approachable and our services are always personal. We offer extensive industry experience alongside a strong desire to stay on top of industry trends and process improvements. Ultimately, we want to make you confident and comfortable in choosing us to be your strategic partner for your manufacturing and product needs.

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Key Competitive Advantages:


  • Emphasis on continuous improvement of quality management system.
  • CMO model that focuses on scale, flexibility, and cost control.
  • Experience and expertise in aseptic processing.
  • Vibrant company culture that represents our passion for the business.

Facility Overviews and Key Characteristics:


  • Approximately 600 employees
  • 40,000 m2 factory compound including 25,000 m2 of production buildings.
  • Three separate production facilities (cleanroom suites) and 10,000 m2 warehouse.
  • Eight high-speed filling lines and 18 lyophilizes with shelves spaces from 20 m2 to 45 m2 to accommodate different scales of productions.
  • Full packaging facility with manual and automatic options.
  • More than 20 contract manufacturing products and seven in-house products. Annual production volume is up to 350 million vials.
  • Competent laboratory facilities for testing, validation, analysis and development.
  • Experience in pharmaceutical engineering management.

 
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