About Segami Corporation

Website
Website
Employees
Employees
11-50 employees View all
Industry
Industry
Medical Device
Location
Location
8310 Guilford Road, Suite A, Columbia, MD 21046, US
Description
Information
Segami is a privately owned US Corporation, founded in 1995 to develop and market affordable, best-in-class, networks of workstations for medical imaging. Segami offers multi-modality clinical applications for most specialties, including Cardiology, Neurology and Oncology. Early on, Segami has earned a reputation as an independent, innovative company, whose products are widely used, in more than 3000 installations worldwide. Segami was the first company in the world to offer medical Imaging workstations based on the Windows platform. Our software is integrated in many fine OEM products serving the Nuclear Medicine and Radiology markets. We also distribute our products through an extensive, worldwide dealer network. The current family of products, named "Oasis" has been designed to always take advantage of the latest state-of-the-art in hardware and software, thanks to its evolutive architecture. Oasis includes a full spectrum of clinical NM and multi-modality applications with a flexible concurrent licensing scheme. With efficient client/server architecture using a centralized application server, Oasis provides uniform reading and processing environment for all of your SPECT and PET cameras. Oasis is a complete vendor neutral software package for general NM, hybrid PET/CT/MR and SPECT/CT studies. Oasis can be integrated into a Hospital environment to enable users from different departments and equipments to communicate and share patient information in a secured manner while maintaining the underlying existing connectivity with the PACS and the HIS/RIS. Segami has developed different customized interfaces to seamlessly integrate with the PACS/HIS-RIS software such that the workflow for the user is transparent and easy. Segami is fully compliant with ISO 13485 quality system, Canadian Medical Device Regulations, European Medical Device Directive and 21 CFR Part 820 US FDA Quality System Regulations.

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