Price: $200
This template serves to provide a comprehensive description of the device, in compliance with the requirements of the Medical Device Regulation (EU MDR) 2017/745. This template serves as a comprehensive guide, providing stakeholders with a clear understanding of the device’s intended purpose, primary function, and key features. Designed to comply with regulatory requirements, the description ensures transparency and accuracy in conveying essential information about the device.
This template is designed by highly experienced professionals for all medical device companies. Click below to get a preview of this template.
