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We care about getting safe and effective medicines to patients
We were created out of the courage to think about the future
Everything we do is supported by our value system
We develop and manufacture biopharmaceuticals
From virtual biotech to the largest pharma
Led by the industry veterans and innovative scientists
Three international centres in Poland & the Netherlands
We have brought over 50 scientists back to Poland
Bringing new & innovative biologics to market
Improving patient access to life saving drugs
Search our open vacancies
Learn why our employees love working here
If you live abroad learn about our beautiful country
We aren’t all scientists, discover what our teams do
Get to know what being part of our team is like
All our latest developments
Presentations, exhibitions, partnering, attendance
Publications, article, brochures and fact sheets
Webinars, explainer videos, corporate films
Interesting articles on the latest developments in biologics
We provide drug product development and cGMP manufacturing of sterile biologicals in liquid and lyophilized forms at lab and large-scale. Our fill finish facility supports vials, cartridges and syringes upto 60 pieces a minute.
Whilst applying a broad array of high-throughput technologies, we provide rapid formulation development accompanied by simultaneous real-time and accelerated stability testing according to ICH standards.
Polpharma Biologics operates a state-of-the-art biopharmaceutical cGMP drug product manufacturing and fill finish plant. The facility is equipped with disposable liquid filling technologies and lyophilization capabilities, and is run by highly qualified and experienced personnel.
Polpharma Biologics method development, qualification and validation for late stage development define the robust control strategy required to manufacture and commercialize biologic molecules.
We utilize a number of advanced techniques to quickly establish processes that will yield the optimal outcome at the highest level of efficiency. We apply quality-by-design (QbD) principles to guarantee the quality, safety and efficacy of your products.
From idea to global supply. We care about getting your product to patients as quickly and safely as possible.
All the component to take your product from DNA, through IND and clinical trials and to support your global commercial supply. This includes antibody discovery, cell line development, process development and cGMP manufacturing supported by extensive analytical capabilities.
State of the art microbial manufacturing facilities for fermentation recovery & purification development through to cGMP manufacturing for preclinical, clinical and commercial supply.
Comprehensive biosimilar development capabilities from cell line development to commercial supply to help our partners provide patients access to the most advanced therapies available.
We utilize our extensive experience in taking products through clinical trials to provide our partners with IP, clinical and regulatory support.
Get in touch for more information.
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