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Strongly reliable and focused Regulatory Affairs Specialist with great breadth of experience in medical device regulatory document preparation and approvals for Class II and Class III devices. Able to handle multiple projects efficiently and accurately. Effective independent worker as well as excellent coordinator with subject matter experts.
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Regulatory Affairs Professionals Society (RAPS)5635 Fishers Lane, Suite 400Rockville, Maryland 20852
raps@raps.org+1 301 770 2920
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