We are a cross-sectional team united by the ambitious goal of revolutionizing the world of diagnostic imaging and having a meaningful impact on people's lives.
Verima brings technology closer to medical knowledge by assisting surgeons and dentists with practical tools for management and holographic visualization of CT and MRI exams by exploiting Mixed Reality and Augmented Reality technologies.
We support healthcare professionals in diagnosing and intervention planning, also making communication with the patient easier.
Clearer diagnostic examinations thanks to true-to-life models
Ability to share clinical cases in the form of holograms at any time, even remotely
Faster time to process 3D models and faster time to act surgically
Gap elimination between doctors and patients
We revolutionize the world of diagnostics
The Verima team consists of software developers, biomedical engineers, UX/UI and communication experts.
The Verima team consists of software developers, biomedical engineers, UX/UI and communication experts.Verima was born in 2018 and is developed by Witapp, a software house based in Florence, dedicated to the creation of digital products involving innovative and immersive technologies.
Technological - Operational Unit
The technological-operational unit consists of a communication team and a team of software engineers who operate using the most advanced programming languages and development software.
R&D Unit - Scientific Product
The R&D unit represents Verima's medical-scientific division, made of biomedical experts specialized in clinical image processing and the development of innovative AI-based solutions.
Verima è un dispositivo sicuro e certificato sviluppato da Witapp
Patent for industrial invention
Verima software holds industrial invention patent No. 102019000003809 filed on 15/03/2019, issued by the Ministry of Economic Development – General Directorate for the Protection of Industrial Property, Italian Patent and Trademark Office. The owner of the patent is Witapp S.r.l.
Verima is a device that complies with the requirements of Directive 93/42/EEC and is therefore placed on the market with the CE markup in accordance with Article 17 of Directives 93/42CEE and 2007/47/EEC.
Class I Medical Device
Verima is a Class I medical device registered to the Ministry of Health under System Progressive No.: 1947525/R.
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