Compliant. Controlled. Convenient.
dokspot is an off-the-shelf eIFU management solution compliant with global eIFU regulations. The product was designed by regulatory experts and software engineers, and provides medical device manufacturers with a controlled and convenient solution to communicating their IFU online.
MDR 23.1 Compliance
With MDR, medical device manufacturers are required to make available and keep up-to-date any device safety and performance information through their company website. dokspot is a standardized solution that allows manufacturers to successfully and promptly address this requirement.
Global eIFU Compliance
With global eIFU regulations, select manufacturers have the option to ship products without paper IFU. dokspot fulfills all additional eIFU requirements, laying the ground for manufacturers to remove the paper-form IFU, reduce process complexity and mitigate risk.
ISO 9001:2015 certified quality management
Validated software with documented releases
Continuously monitored for availability
SSL encryption and integrity protection
No development, setup, or infrastructure investment
No technical resources for operation and maintenance
Integrates into website and corporate identity
Expandable to all types of product resources
dokspot is a Swiss based software-as-a-service company focused on eIFU for medical devices. Since 2014, international manufacturers trust dokspot to securely and reliably communicate the IFU of thousands of medical devices through manufacturer-branded eIFU websites.