Rigorous and detailed verification and validation testing are necessary to demonstrate that Medical Devices meet their technical requirements, fulfil user needs, and are effective for their intended use. Robust process validation ensures that the manufacturing and sterilization processes consistently produce products that meet the requirements. Your verification and validation records will be indispensable for future regulatory clearance, certification, and registration, and will be scrutinized by the regulatory authorities during the approval process. So it is essential that the verification and validation are thorough, scientifically sound, and done right the first time.