New UDI Regulations, Global Labeling Requirements Among Discussion Topics at Second Semi-Annual Meeting
(Chicago) – The 2nd Semi-Annual Medical Device and Diagnostic Labeling Conference will be held April 30-May 1, 2015 in Arlington, Virginia, offering labeling and regulatory affairs executives an exclusive opportunity to discuss the latest compliancy and regulatory requirements enacted by the FDA, as well as both domestic and global practices.
The conference, hosted by Q1 Productions, will offer sessions, panel discussions, and interactive small group workshops led by some of the industry’s leading experts, as well as a wide variety of topics on best practices and challenges. Speakers and panelists, including Dawn Fowler of Endologix, Melissa Finocchio of Biomerieux, and Jackie Elkin of Medtronic, will be on hand for extensive networking opportunities and to offer insight to UDI regulations, GUDID compliance, evolving global labeling requirements, and much more.
This year, conference delegates will have multiple opportunities for small-group discussion to address specific industry challenges and exchanging strategies and insights. An industry-specific breakout session will allow executives to discuss issues within their sector such as labeling development, data, and compliance, as well as provide a platform for exchanging tips and strategies. In addition to open floor workshops and networking opportunities, delegates will also take part in an interactive SPL Workshop, led by Gary Saner of ReedTech, which will allow for a hands-on approach to Structured Product Labeling, how to mitigate and correct errors in formatting and ensuring a streamlined approach.
For more information on the 2nd Semi-Annual Medical Device and Diagnostic Labeling Conference, please visit www.q1productions.com/labeling, or contact marketing@q1productions.com.
