RAPS Healthcare Device Submission and Compliance Workshop to Function FDA Regulators, Business Professionals


Rockville, MD (PRWEB) February 28, 2013

The Regulatory Affairs Pros Society (RAPS) will host a two-day workshop on medical device submissions and compliance that will bring together professionals from business and officials from the US Meals and Drug Administration (FDA) to address how device makers can function much more effectively with FDA and meet evolving regulatory expectations. The workshop, Healthcare Device Submission &amp Compliance Techniques for the US Market, will be held 78 March at the USP Meeting Center in Rockville, MD, USA.

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