medical device design software
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ISO 13485 Automation Path Software
Vintara’s Enterprise Portal helps leaders deploy world class best practices for the manufacture and sale of medical devices. Our configurable workflow applications will drive performance and world class regulatory compliance including: ISO 13485, 21 CFR Part 11 compliance, 21 CFR Part 820 compliance, ...
By Vintara based in Oakland, CALIFORNIA (USA). from Automation Path Software line
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RegScan - Version MDR - Medical Device Reporting System
The medical device reporting (MDR) requirements of 21 CFR 803 apply to manufacturers, importers, distributers, and device user facilities in the United States. Such facilities are required to report adverse device-related events to the Food and Drug Administration (FDA) or the device manufacturer, and ...
By RegScan, Inc. based in Williamsport, PENNSYLVANIA (USA). from Quality Suite Checklists Software line
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RAPID ANEURYSM - Software for Comprehensive Aneurysm Management
Rapid Aneurysm is an FDA-cleared imaging platform for cerebral aneurysm management. Helping physicians save time, improve patient care, and increase revenue by automating the process of finding, tracking, and proactively treating aneurysms. From a patient’s imaging scans, the platform creates a personalized 3D model of the vasculature and provides tools for accurate measurement and ...
By RapidAI based in San Mateo, CALIFORNIA (USA).
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Medical Robotics Software
, electronics, and embedded engineering expertise for these types of projects. Our medical robotics group includes embedded developers with graduate computer science and EE degrees. Experience is deep: whether handling precision movement at the micron level, multi-axis movement optimization, or designing custom ...
By Syncro Medical based in Langhorne, PENNSYLVANIA (USA).
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BrightInsight - Starter Assets Software
Accelerate your time to market and reduce development costs with our pre-built Patient App and Clinician ...
By BrightInsight, Inc based in San Jose, CALIFORNIA (USA).
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