Medical Device 2015 - Medical Device Registration & Listing, and Inspection Follow-up Activities

Overview:
Companies need to remain vigilant in understanding and applying current FDA law and regulation pertaining to the marketing of their devices in the US. Failure to do this raises their regulatory risk and hampers their ability to stay competitive in the rapidly advancing technological world of medical device manufacturing and marketing. The stakes are made even higher as device regulatory authorities around the globe are harmonizing their regulatory standards and requirements while increasing their collaborative efforts to ensure product safety.
This webinar will explore key concepts in helping your company stay ahead of the regulatory curve by understanding FDA operations and developing effective mitigations to reduce risk, wherever your devices are marketed around the globe.
Why should you Attend: Many companies struggle with understanding how FDA makes decisions on how to regulate medical devices that are being marketed. This includes not understanding how FDA uses registration and listing data for inspection planning to not knowing how they assess CAPA and complaint problems. In some cases, companies fail to manage inspections to reduce the risk of adverse findings, and they fail to address key issues in response to 483s and Warning Letters.
Here is your chance to better understand how FDA thinks and operates and what their key areas of focus and priority are from a former Compliance insider.
Compliance4All
Adam Fleaming
Phone: +1-800-447-9407
Event Link: http://www.compliance4all.com/control/w_product/~p...
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