Pharmaceutical professionals recognize that selecting a reliable active ingredient manufacturer is one of the most important aspects of drug development. The chemists and sourcing specialists at Frontage have experience and met the challenges of supplying reliable, pure and FDA-approvable ingredients. In conjunction with our international suppliers, GMP production of API's is managed with a quality system modeled after ICH Q7A and FDA requirements. Frontage personnel have been involved in more than 30 FDA inspections of API manufacturing facilities within the last several years, so you can be assured that our quality system addresses issues such as cleaning, change control, equipment validation, and raw materials controls. With our broad experience in various reaction pathways and with the identification, separation and characterization of impurities, Frontage's clients rely on consistent delivery of high quality products. Frontage Laboratories, Inc. is more than a contract laboratory... we're a collaborative R & D company dedicated to advancing the development efforts of pharmaceutical companies around the world. We specialize in assisting our partners through decades of technical experience in major pharmaceutical companies and offer quality services, rapid turnaround time and competitive pricing. You can also contact our local offices for your needs in pharmaceutical research and development projects: Bioanalytical Services ? Bioanalytical method development, validation and sample analysis supporting preclinical pharmacokinetic, toxicokinetic, and clinical pharmacokinetic studies Pharmaceutical analysis ? method development, validation and testing Formulation development ? injectable and oral liquids, oral capsules and tablets For further information, please visit our web site at www.frontagelab.com