DeviceAlliance March mixer covers ‘FDA no no’s’

February 27, 2017 By Danielle Kirsh

DeviceAlliance will be presenting a Special Speaker Engagement with Carla Wiese, principal medical research scientist at NAMSA, at a March 15 mixer.

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.

DeviceAlliance
devicealliance.org

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About The Author

Danielle Kirsh

Danielle Kirsh is an award-winning journalist and senior editor for Medical Design & Outsourcing, MassDevice, and Medical Tubing + Extrusion, and the founder of Women in Medtech and lead editor for Big 100. She received her bachelor's degree in broadcast journalism and mass communication from Norfolk State University and is pursuing her master's in global strategic communications at the University of Florida. You can connect with her on Twitter and LinkedIn, or email her at [email protected].