In this highly interactive, hands-on Regulatory Strategy Forum, proven experts from the medical device industry will lead you in engaging discussions and interactive case studies analyses that will give you the insight and tools you need to develop a successful global regulatory strategy.
In addition to gaining an appreciation for global differences in submission formats and filing strategies and an understanding of the critical importance of monitoring and revising your strategy, you will examine such vital subjects as:
Knowing how to develop an effective global regulatory strategy is an essential skill for regulatory professionals. Successful global regulatory strategies maximize commercial opportunities for healthcare product manufacturers while minimizing company risk. By engaging in in-depth analysis and workgroup collaboration, you will gain a thorough understanding of ways to enhance your strategy and further your product’s success.
Mid-level regulatory professionals from industry and consulting firms planning international submissions.
Regulatory Affairs Professionals Society (RAPS)5635 Fishers Lane, Suite 400Rockville, Maryland 20852
raps@raps.org+1 301 770 2920
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