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Alexander Varond is presenting at the FDLI, Introduction to Medical Device Law: Registration and Listing
June 16, 2015

June 16-17, 2015 | Hunton & Williams LLP | Washington, DC

Are you conversant on the Food and Drug Administration’s (FDA) regulation of medical devices? More importantly, do you and your organization know how to comply with these regulations? Participating in this two day training course can help you understand FDA regulations, support your efforts to get products approved, help minimize regulatory problems and know when FDA is likely to allege violations of the law. This in-depth, interactive two-day course is beneficial for new professionals in the medical device industry or seasoned regulatory affairs or legal professionals looking for a refresher on current FDA medical device policies and practices. Attendees will hear from and interact with experts who will review the essential elements of medical device regulation.

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