The topic of the mixer will be “FDA No No’s” and will cover the common pitfalls that companies should avoid when submitting a 510(k) submission. As a former lead reviewer for the FDA, Wiese has the expertise to help companies get their submissions through in a more timely and efficient manner.
The event will take place on March 15 from 5:30 p.m. to 7:30 p.m. at The Vine in Irvine, Calif. DeviceAlliance members can RSVP for no charge online. Non-members can attend by applying online and paying a fee.
Visit http://www.devicealliance.org/events.html for more information and to register.
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