As a 175-year-old American company, we’re proud to lead the world in medical innovation. Our U.S. supply, manufacturing, and distribution sites are focused on ensuring that all Pfizer products are made to the highest standards of quality, safety, and efficacy.
Since 1982, the Middleton site has focused on the manufacture of biologics. The 83,000-square-foot facility isolates bovine thrombin, a naturally occurring enzyme which plays a critical role in rapid clotting (hemostasis) of blood.
The North Creek site, integrated into Pfizer’s network following the Seagen acquisition, produces antibody drug conjugates (ADCs) and antibody intermediates.
With more than 100 years of rich history in innovation and manufacturing excellence, 19 products- including various vaccines, antibiotics, and oncology medicines, have been discovered, developed, and approved at the Pearl River, New York site.
Once operational, the Sanford North facility will have the capabilities for producing biologics.
How Drugs Are Made
The medicines available today have taken an average of 12 years to develop. With dedication, creativity, and science, we can significantly cut that time.