KP Pharmaceutical Technology, Inc. (KPPT) is a privately-held Contract Research Organization (CRO) and a full service cGMP certified manufacturer.
KPPT has dedicated manufacturing areas with independent HEPA/HVAC air handling and dust containment systems, and 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. They also 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.