A leading Contract Research Organization (CRO) and a full service cGMP manufacturer (CMO), KP Pharmaceutical Technology, Inc. (KPPT), is a privately held corporation 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 modern analytical instrumentation required for raw material and finished product release testing and stability studies as per cGMP and ICH guidelines.
We have capabilities for developing and manufacturing oral, topical, as well as sterile dosage forms including potent/cytotoxic and DEA scheduled drug substances. Our qualified state-of-the-art, sterile aseptic fill and finish manufacturing facility with class 100/ISO-5 certified clean rooms can manufacture all types of sterile dosage forms including, lyophilized formulations; sterile suspensions and emulsions, sterile powder filling, sterile spray products; ophthalmic and otic formulations. Terminal sterilization services are also available if needed.
Our facility is one of only few to offer a wide range and scope of services in the industry today. We work closely with clients and have the capabilities to develop and produce virtually any type of pharmaceutical dosage form.
We are a reliable, market driven, entrepreneurial company that understands the necessity of cost effective R&D and production of highly time sensitive clinical supplies. Every effort is made to ensure rapid and efficient service, from quotation to delivery.
All projects are executed under complete confidentiality, client-specific needs and in compliance with cGMP