Microbial fermentation manufacturing

State of the art cGMP facilities for microbial fermentation

We have state-of-the-art facilities for microbial fermentation manufacturing. These physically separated suites are operated by dedicated staff for preclinical, clinical and commercial manufacturing.

Microbial manufacturing capabilities

We have built a modern and fully integrated environment for the development and production of biological medicines using microbial expression systems. Through working on our own pipeline, we have gained invaluable expertise, insights and experience.

Polpharma Biologics is led by a team with decades of international experience and a proven track record in biologics development, clinical and commercial production, registration and commercialization. All our activities will be supported by our Quality Control and Quality Assurance department.

Microbial manufacturing capacity

  • Physically separate microbial production suite operated by dedicated staff
  • cGMP fermentation scale of 500 L/batch (nominal volume) for clinical and commercial supply
  • Upstream process including primary recovery in stainless steel technology
  • Downstream process in single-use technology for fast changeover and zero cross-contamination risk
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Drug product and fill finish

Polpharma Biologics provides drug product development and cGMP manufacturing of sterile biologs in liquid and lyophilized forms at lab and large-scale. See our full range of drug product services.

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Working with our manufacturing group

“We are committed to positive outcomes and delivering projects on time to specification”

Our extensive capacity means we can transfer in external processes or continue with integrated projects. We understand that we are delivering material for pre-clinical, clinical trials and for patients in urgent need of treatment, we always endeavor to get your product to where it needs to be.

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Let’s collaborate and create quality biologics together.

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