While design control has been a quality system requirement since 1996, many medical device organizations struggle to understand these requirements, as well as when to start the process and how to maximize the benefits of the system. For example, it is often mistaken that a design control process must be complex to meet the regulatory requirements and to ensure delivery of a safe product that meets customer demands. Additionally, another common mistake made by device manufacturers is initiating the design control system process later in the overall design process.
Understanding the elements of design control will help a company focus on the important aspects of the product while reducing the risk to the patient and getting the device to market faster and more efficiently. By attending this webinar, you will learn how to get the most from your design control process.