Discover the science behind our biologics production

Collaborating with Pfizer CentreOne makes peace of mind possible. We give you access to the technical expertise and regulatory track record of a partner that has walked in your shoes and understands the challenges you face. Let us help you reach your key milestones with an altogether different approach.

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A solid foundation for success

Partner with us for your large molecule biologics manufacturing and leverage our many years of experience. Using expression in recombinant organisms including vaccine drug substances and intermediates, therapeutic proteins, and monoclonal antibodies (mAbs) and mAb biosimilars, we have the expertise to help you achieve true peace of mind.

We harness the power of single-use technologies to deliver greater speed and efficiency, additional assurances of eliminating cross contamination, as well as streamlined cleaning validation and process simplification.

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Your gene and cell therapy innovation brought to light

Time is life and experience is key with gene and cell therapy, so choosing the right CDMO partner is critical. 

With a global team of Pfizer gene and cell therapy scientists and manufacturing experts, we have the experience in developing and manufacturing scalable viral vectors across multiple serotypes, in a significant number of GMP batches with proven quality control.

Our extensive network of global regulatory experts, analytical and quality control engineers, means that we can help you overcome bottlenecks and troubleshoot. We are ready to help ensure your innovation reaches your patients fast.

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Mastery in tech transfer, process optimization and scale-up

Our experts take an open and collaborative approach to exploring ways of optimizing the manufacturing process. Our analytical, engineering, chemistry, and microbiological specialists are always transparent with you, remaining available to answer your questions and ensure your products are manufactured as efficiently as possible to the highest quality.

Our robust tech transfer process maintains consistency and quality in commercial manufacturing.

Integrated facilities

Leveraging Pfizer's Global Manufacturing Network, we can deliver upstream and downstream drug substance manufacturing combined with sterile fill finish for drug products at one location, with an integrated, scalable program. Our experts partner with development teams to enable seamless integration across the entire lifecycle of your molecule, from development to commercial manufacture.

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Capabilities at a glance

  • Lyophilization of intermediates
  • Raw material sourcing
  • Cell bank storage
  • Wave expansion
  • GE X cellerex XDR 2000 bioreactor
  • Viral filtration
  • Tangential Flow Filtration (TFF)
  • Chromatography
  • Extractables and Leachables (E&L) studies
  • Comprehensive sterile filling capabilities including lyophilization and pre-filled syringe
Let’s collaborate