5 Mistakes That Can Turn Your Product Registration Into a Money Drain

by Carl Ning

Medical device registration may seem straightforward but is actually prone to potentially costly mistakes. 

Medical device organizations are required to register medical devices with notified bodies in all countries where they sell those products. This process is fairly well understood and expected.

However, there are pitfalls in the practice of compiling the dossiers to register, and mistakes can end up costing a company money, according to Carl Ning, director of global solutions architecture for Sparta Systems (Hamilton, N.J.).

Ning highlighted the common errors medtech companies make in thinking about product registration and offered some solutions:

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