This medical device webinar will discuss the FDA guidance on Mobile Medical Applications and provide clarification on the primary points of the guidance.
Why Should You Attend:
In July 2011, FDA published a draft guidance entitled "Mobile Medical Applications”. This guidance was issued on September 25, 2013 and, though not binding, it reflects FDA’s current thinking on use of mobile applications as medical devices.
Who Will Benefit:
This webinar will provide valuable assistance to following personnel in the medical device industry:
Staff involved with regulatory filings
Product Development managers
Mobile and Smartphone Companies
Cheryl Wagoner, has 20 years of experience in quality assurance, and regulatory affairs. She currently is the Principal Consultant/Owner of Wagoner Consulting LLC, where she provides consulting services to medical device and pharmaceutical companies. Previously, she has held various positions in Quality, Regulatory, Clinical and Compliance in the medical device and pharmaceutical industries.
Use coupon code 232082 and get 10% off on registration.