A Premier CDMO. FDA Registration #1210580.
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Denison Pharmaceuticals maintains established procedures and activities to monitor, measure, analyze and improve processes required to ensure quality across the entire company.

Such activities include internal audits, review of data, control of non-conforming data, and monitoring of events that could directly influence the quality and of the products manufactured at Denison Pharmaceuticals.

Denison Pharmaceuticals is regularly inspected by regulatory authorities, including the U.S. Food and Drug Administration, Drug Enforcement Administration as well as frequent ongoing audits from existing and new customers. We welcome these audits and incorporate any feedback received from continuous improvements to our Operations and Quality Systems.

In addition, Denison Pharmaceuticals is committed to continuous investments in our plant, technologies, and equipment. We provide our employees with ongoing cGMP compliance and regulations including FDA, EPA, USP and ISO guidelines. Our Quality System staff has a wide range of solid experience working in the
pharmaceutical industry.