This webinar discusses establishing a reduced testing program for incoming components in accordance with GMP quality principles and regulations. It will review the reduced testing lifecycle, including specifications, supplier qualification, auditing, and validation. Examples will demonstrate how to design systems to reduce costs while ensuring compliance. Attendees will learn how to qualify suppliers, control specifications, and reduce testing while maintaining quality. The speaker has 30+ years of experience implementing quality systems and will discuss applying quality assurance principles to medical devices and pharmaceuticals.