Use this Verification and Validation (V&V) Plan template to systematically document and organize all planned verification and validation activities for your medical device, including hardware, software, packaging, shipping, electrical safety, and biocompatibility testing. This template is essential for demonstrating compliance with regulatory requirements and industry standards during design and development, and should be filled out prior to initiating V&V testing to ensure all protocols, responsibilities, and acceptance criteria are clearly defined and approved. Completing this document provides a comprehensive foundation for regulatory submissions and quality audits by ensuring every aspect of product testing and validation is planned and traceable.