Description
The Design Verification Plan Template is a critical document utilized in accordance with ISO 13485, an international standard for quality management systems in the medical device industry. This template serves as a structured framework for planning and executing the verification activities necessary to confirm that the design outputs meet specified requirements. It outlines the objectives, methods, acceptance criteria, and responsibilities for each verification activity throughout the design process. By using the Design Verification Plan Template, medical device manufacturers can ensure that all design verification activities are systematically planned, documented, and executed to demonstrate compliance with regulatory requirements and achieve product quality objectives.
