Sponsor or Organizer: Compliance Trainings
Description: This webinar will provide an opportunity to get familiar with an FDA's process to communicate with the industry early in the process for sustainable 510(k) preparation and submission.
This webinar is intended to discuss what and how to obtain FDA feedback on your proposed questions, which will be helpful and useful for your device design, preclinical and clinical study plan and design, if applicable.
Dates: 03/04/2014
Location:
Mississauga, Ontario, Canada
|