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Introduction

This webinar is intended to demonstrate how to put together a compelling (bullet proof) 510(k) in compliance with the FDA's eCopy and RTA policy so that your time, energy and financial resources can be effectively used to expedite your 510(k) clearance, potentially leading to saving millions. In September, 2013, FDA has cleared 211 devices (510(k)s) under the 510(k) program. Among those, there were nine (9) abbreviated and 41 special 510(k)s. Two of these 510(k)s were initially submitted in the middle of the year 2011.

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Venue

online

online, 201,N Squirrel road,, Auburn Hills,, Suite 1007,, michigan., 48326., United States

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Organised by

Global Compliance Trainings

Contact information

Mr john gordan
201,N Squirrel road, Suite 1007, Auburn Hills, Suite 1007,, Auburn Hills,, michigan., 48326., United States of America
2482120588
Contact us by email

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