Start/End: 06-08-2009 — 06-09-2009
Do you know how to get your devices approved while avoiding common pitfalls and costly delays? Medical device companies must have FDA 510(k) approval to market products in the United States. Learn the best way to get your approval to market in the U.S., what is needed to complete the 510(k) process, and when a 510(k) must be submitted. Our 510(k) process training, presented by industry experts using hands-on workshops, covers the requirements needed so you can get your product on the market.
Understand how to submit a successful 510(k) for a device or a device change as quickly and efficiently as possible to avoid regulatory issues and unnecessary expenses. Make sure your 510(k) submission can be quickly reviewed by the FDA so you can stay ahead of the competition.
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Hotel TBD. Also available to be held at your facility.