As a global CDMO powered by Pfizer, Pfizer CentreOne leverages 20+
years of antibody drug conjugate (ADC) innovation. Backed by a world-class
manufacturing facility in Pearl River, NY, we are ready to help you
get your therapy from clinical to commercialization at speed to answer
patients’ needs.
We harness a strong track record of ADC success, including producing the
world’s first commercially approved ADC product (MylotargTM), to drive
advancement and help us achieve better ADC solutions together.
Unravel the complexities of ADC development and manufacturing in our whitepaper.
Accelerate your ADC development with our end-to-end support, in our brochure.
Discover our biologics development and commercial manufacturing expertise
Leveraging approximately 24,000 square feet of ADC manufacturing space specifically designed for highly potent and cytotoxic drug processing, the Pearl River, NY, site is ready to unlock the bio-logical brilliance of your project.
In ADC development and manufacturing, unraveling complexities is key because time is life.
As an experienced global CDMO partner, powered by Pfizer, we can help you skillfully maneuver ADC challenges, keeping pace with scientific advancements and regulatory requirements.
Responsible for technical transfer and validation of ADCs and immunoconjugates, Dave has over 20 years of experience in commercial and clinical manufacturing to support you throughout your journey.
Lisa Thimmesch has over 20 years of experience supporting Pfizer CentreOne’s customers with regulatory inspection compliance, aseptic and lyophilization manufacturing expertise, quality systems and contract manufacturing quality leadership.