USBIMED has deep knowledge about regulatory requirements relative to medical devices (including software, digihealth), as well as safety related user interface design and usability requirements. Different actors of health tech domain benefit from high quality in house medical device regulatory and usability training, sparring and expert services. Digital Health, mHealth and standardization are speciality areas USBIMED contributes as well.
●Support and training services for medical device or software usability requrements, processes and methods
●Regulatory affairs training packages and sparring
●mHealth services for industry, assesment framework developers and healthcare units
●Expert article writing for professional publications and other media. Expert presentations at events.
●Advisory board, mentoring and steering group tasks for associations or research projects
Consultancy services for health industry, Creative Industries, Design services, Health & Life Science, Health technology and eHealth, ICT, SW-development, Testing and Certification Services
eHealth, HealthTech, Service Design