Medical Device Validation and Verification (V&V) are critical processes that play a vital role in ensuring the safety, performance, and regulatory compliance of medical devices throughout their lifecycle. With the advancement of medical technologies, particularly those that rely on software, the importance of comprehensive verification and validation (V&V) processes is increasingly significant for manufacturers, regulators, and healthcare providers. This heightened focus ensures that these technologies meet safety and efficacy standards, ultimately benefiting patient care. Specifically, verification checks that a device is manufactured according to design specifications, while validation confirms that it performs its intended clinical function safely and effectively for users.