Founded as Integrity Biosolution in 2003, Integrity Bio Inc. has been offering formulation development services since its inception. The company Integrity Bio Inc. has become one of the largest designing and constructing Good Manufacturing Practices (GMP)-compliant parenteral manufacturing facilities. The company develops, transfers, qualifies and validates many assays from Total Organic Carbon (TOC) to High Performance Liquid Chromatography (HPLC), and beyond. Its core business of formulation development has successfully served both early-stage companies and several of the world's largest biotechnology, pharmaceutical and medical device companies. The contract manufacturing services offered by Integrity Bio Inc. are formulation development, GMP fill-and-finish, stability studies and testing.
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