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MDUFA 2012<br><i>First-Hand Knowledge for Medical Device Companies</i>
Registration
Audio CD/Transcript - Aug. 9, 2012
$327.00
Audio CD/Transcript - Aug. 9, 2012
$327.00
When
Event Description
In this special 90-minute webinar, former FDA Deputy Associate Commissioner for Regulatory Operations Steve Niedelman and Partner in the FDA & Life Sciences Practice at King & Spalding, LLP, attorney Pamela Furman Forrest, will provide essential guidance on the recently enacted FDA Safety and Innovation Act and revisions to the medical device user fee authorization that will affect the medical device industry. They’ll provide strategies on achieving compliance, describe what new procedures and requirements devicemakers will face, as well as discuss what companies can expect the FDA to deliver during the next five years.