Integrity Bio, Inc. was originally founded as Integrity Biosolution in 2003. Offering Formulation Development services since its inception the company quickly endeavored into the large project of designing and constructing GMP compliant parenteral manufacturing facilities in an adjacent building to the research laboratory. After commissioning and validation were completed the first of many successful cGMP manufacturing campaigns were launched in 2007.
Since that time many additional services and improvements have been made to support that operation. The addition of cGMP Stability Programs to service our existing clients was a great success and prompted the expansion of our GMP Quality Control Laboratory. We have developed, transferred, qualified, and validated many assays from TOC to HPLC and beyond. Most recently the addition of Ultra-Filtration / Dia-Filtration (UFDF) via Tangential Flow Filtration (TFF) has been added to our list of capabilities. This provided the ability to "Turn Key" most clients' projects from Formulation Development through Clinical Trials.
All these changes and improvements prompted the new name and logo. So in November of 2009 we became Integrity Bio, Inc.