Claio is a data management software designed for operations and managements in healthcare facilities. This specialized software prevents possible losses of data while centralizing patients’ health records from respective medical devices. Claio also delivers healthcare professionals benefits of digitalization which frees them from tremendous paperwork, significantly changing their workstyles and performances.
GAP is an innovative, near-objective perimeter designed to detect early-stage symptoms of eye diseases like glaucoma. It minimizes the impact of individual judgment or interpretation through the use of eye tracking technology and AI-based testing logics. With this device there is no need for a patient to fix the eyes or to press the button as the visual field is automatically measured when the patient follows the stimulus with both eyes. Notably, this device is a head mounted display, that allows users to carry it around, and to administer the test outside the dark room. GAP is a PMDA*1 licensed and EU-MDR*2 conformed medical device and has already installed to eye clinics within Japan, since its domestic launch in April 2021.
*FIELDNavigator is an OEM product of our perimeter GAP, distributed by Rexxam Co., Ltd.
C-Note is a software that solves the problem of medical record entries in medical fields where it is difficult to make sufficient medical record descriptions using only the template function of an electronic medical record. Especially in ophthalmology, otorhinolaryngology, and obstetrics, medical articles can be written without stress by freely arranging images, numbers, text strings, etc. as in a traditional paper medical record.
DocuMaker is a painless solution to complicated paperwork in healthcare facilities. This software not only automates tedious tasks in documentations but also improves quality of data and speeds administrative operations. With its accuracy, DocuMaker functions as a database. Registered users can generate documents from previous medical records and patient information from other connected software. Stored information can also be utilized for data statistics and analysis.
*1 Pharmaceuticals and Medical Devices Agency (PMDA) is an independent administrative agency in Japan that provides guidance and reviews the quality, efficacy, and safety of pharmaceuticals and medical devices from pre-clinical to approval, and collects, analyzes, and provides safety information after market launch, contributing to the improvement of public health.
*2 European Medical Device Regulation (MDR) is a new set of regulations that governs the production and distribution of medical devices in Europe, and compliance with the regulation is mandatory for medical device companies that want to sell their products in the European marketplace.