Chelsea Becker Email and Phone Number

10+ years in Regulatory Affairs experience, 5+ years of regulatory people management experience, and Regulatory Affairs US Certified (RAC) through RAPS. I currently specialize in Class I and II medical devices in the U.S., in which I have authored and received clearance for many 510(k) submissions to the FDA. I also specialize in Class II and Class III medical devices in the E.U., in which I have maintained technical documentation and authored change notifications to the notified body.