Question: What are the federal requirements for reporting adverse events related to medical devices? Answer: Under the Medical Device Reporting (MDR) regulation, 21 CFR 803, device user facilities are required to report...
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What our customers are saying about us… New Features Announcement - …excellent additions to the product and right on track with our needs. (Health System in California)  I would like you to...
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MCN Healthcare staff give back in a variety of ways during the year. One of our clinical staff recently travelled to Madagascar through the Lutheran Church Missouri Synod. This group sends...
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