KRS is an industry-leading customized FDA registered and inspected 503b Human Outsourcing Facility, that provides sterile and non-sterile compounding services to patients, surgery centers, ophthalmology clinics, hospitals and universities nationwide.

KRS commits to compliance with FDA guidelines and guidances. KRS commits to quality, patient safety, and setting the ethical standard for all other 503b outsourcing facilities. KRS is registered with the FDA as a DEA Manufacturer and holds State Board of Pharmacy licenses both in-state and out-of-state. KRS follows all applicable cGMP requirements and meets or exceeds USP Chapter <797> requirements. Our products are recognized as superior preparations due to our process validations that mirrors that of a pharmaceutical manufacturer. Our quality assurance mirrors that of a full analytical laboratory by providing certificates of analysis on all sterile preparations.

KRS is much more than just a supplier of sterile compounded products. The clinical pharmacists at KRS also provide guidance to their clients on the proper handling of sterile products, regulatory requirements regarding sterile products, and clinical expertise in the use of the products they prepare.

KRS pharmacists and staff are available to answer your questions, anytime! We are here to help you with timely answers to formulation questions, product availability, clinical assistance and anything else related to sterile injectable products.