Process Validation has been a requirement in the Medical Device field for many years, however few organisations have embraced the full potential of this requirement to the betterment of not just compliance but also to improved business performance. A solid program for Process Validation, in addition to providing regulatory compliance, also provides optimum equipment performance, consistant process yield, improved internal customer experience and overall reduced production costs. Process Vaidation on legacy prodcution , in addition to new product and process introduction, validation of supplier processes, and product transfer to a new facility or to a contract manufacturer all present opportunity for compliance risk and cost to your business. With considerable experience in Process Validation and Optimisation, Auxilium can contribute not just to your compliance profile but also bring value to your organisation.