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Medical Case Reports Software In Usa New Jersey
2 software items found
by:Honeywell | Life Sciences based inHamilton, NEW JERSEY (USA)
Medical device manufacturers must comply with 21 CFR Part 820, medical device reporting (MDR), premarket notification 510-(k), investigational device exemption, and quality system (QS) regulations. Audits help manufacturers to improve quality, lower costs, and increase compliance. But, managing them manually can become a time and resource intensive ...
Manufactured by:VectraCor based inTotowa, NEW JERSEY (USA)
Office Medic software improves workflow by having one platform for ECG and Spirometry testing. Office Medic allows you to acquire, store and review diagnostic data using an off-the-shelf laptop, desktop or tablet. It increases efficiency, improves patient care and reduces costs. It puts diagnostic testing right at the point-of-care and delivers that information instantly and ...