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ivdrift skip to content home datancia com menu home datancia com ivdrift is now ivdwise the name has changed but our mission has not ivdwise we chose ivdwise because successful ivd development is about making the right decisions at every stage from study design to regulatory submission it reflects the expertise and scientific judgment behind our platform and consulting services effortless compliance every time ivdrift ensures your documentation is always fully compliant with regulatory standards no more second guessing or manual checks just accurate and reliable reports ready for submission with clear prompts and structured workflows compliance becomes straightforward allowing you to meet every requirement without hassle boost efficiency focus on innovation ivdrift handles the heavy lifting of regulatory documentation allowing you to work faster and more efficiently by automating compliance tasks you can focus on driving innovation and product development knowing your submissions are accurate and ready for approval stay ahead while we manage the details minimize human errors ivdrift reduces the risk of human error by automating critical compliance checks and data verification it ensures that every section of your documentation is accurate complete and in line with regulatory requirements by streamlining complex tasks the tool allows you to avoid costly mistakes and speeds up your submission process with confidence knowledge management in one place ivdrift consolidates all your company s regulatory knowledge into a single organized platform with oversight from our regulatory experts your documentation and internal processes are kept accurate up to date and easy to access no more scattered information everything you need is at your fingertips ensuring consistency and compliance across the board products ivdrift analyze ann ensure compliance in ivd product validation and verification with our software designed to automate statistical analysis customize regulatory reports and standardize procedures to meet rigorous european ivd regulations discover more ivdrift regulate ai regina generate compliant documentation with our ai powered tool which compiles verifies and organizes data from diverse sources into comprehensive reports streamlining collaboration and ensuring regulatory accuracy discover more ivdrift check ai chelsea provide a thorough final review pinpointing any areas that require attention for eu 2017 746 compliance so you can submit your technical documentation with confidence coming soon products ivdrift analyze ann ensure compliance in ivd product validation and verification with our software designed to automate statistical analysis customize regulatory reports and standardize procedures to meet rigorous european ivd regulations discover more ivdrift regulate ai regina generate compliant documentation with our ai powered tool which compiles verifies and organizes data from diverse sources into comprehensive reports streamlining collaboration and ensuring regulatory accuracy discover more ivdrift check ai chelsea provide a thorough final review pinpointing any areas that require attention for eu 2017 746 compliance so you can submit your technical documentation with confidence coming soon a team of experts our software is developed by a dedicated team of professionals from both academia and industry bringing together extensive expertise in statistics regulatory compliance and applied problem solving with a deep understanding of real world challenges our team is uniquely equipped to bridge the gap between cutting edge research and practical solutions for ivd manufacturers in addition to building the software we offer on demand consultancy services combining our educational spirit with regulatory insight to help address your specific needs with precision and clarity our origins previous next ai assisted highly compliant technical documentation preparation for ivd medical devices quick links home terms and conditions privacy policy cookie policy eu home terms and conditions privacy policy cookie policy eu get in touch c saragossa 47 1r 08006 barcelona phone 34 630 725 232 ai assisted highly compliant technical documentation preparation for ivd medical devices quick links home terms and conditions privacy policy cookie policy eu home terms and conditions privacy policy cookie policy eu get in touch c saragossa 47 1r 08006 barcelona phone 34 630725232 manage consent to provide the best experiences we use technologies like cookies to store and or access device information consenting to these technologies will allow us to process data such as browsing behavior or unique ids on this site not consenting or withdrawing consent may adversely affect certain features and functions functional functional always active the technical storage or access is strictly necessary for the legitimate purpose of enabling the use of a specific service explicitly requested by the subscriber or user or for the 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