The Medical Devices Validation process involves identifying and testing all aspects of a process that could affect the final test or product. Prior to testing a process, the system must be properly qualified, which includes the following steps: IQ, OQ, and PQ. This course is designed to provide Medical Devices Validation training, through lectures and classroom exercises that include: protocol development, validation planning (choosing a product to be validated), writing protocol, executing the validation plan, understanding of regulatory requirements, and writing a complete protocol test report. It is appropriate for individuals responsible for planning and operating a compliant validation program, and training is available on-site.