KP Pharmaceutical Technology, Inc (KPPT) - nicht nehmen, doppelt A leading Contract Research Organization (CRO) and a full service cGMP certified manufacturer, we started operations in 1997 in Bloomington, IN. At KPPT, we have dedicated manufacturing areas with independent HEPA/HVAC air handling and dust containment systems. We also have a complete in-house, independent QC Laboratory fully equipped with all modern analytical instrumentation required for raw material and finished product release testing and stability studies as per cGMP and ICH guidelines. We have the capability for developing and manufacturing oral, topical as well as sterile dosage forms. Our qualified state-of-the-art, sterile / aseptic fill and finish manufacturing facility with class 100 clean rooms can manufacture and test all types of parenteral (sterile) dosage forms, including lyophilized formulations. Terminal sterilization can also be performed if required. Our facility is one of only a few centers to offer the range and scope of services needed by commercial clients. We work closely with clients to develop and produce virtually every type of pharmaceutical dosage form. We partner with large and small pharmaceutical firms from around the world to develop and produce new pharmaceutical agents for use in human clinical trials as well as commercial manufacturing.