Brooke Robinson possesses extensive experience in regulatory affairs, currently serving as Manager of Regulatory Affairs at SetPoint Medical since February 2022, following a progression from Sr. Regulatory Affairs Specialist. Prior experience includes roles at Experien Group, where responsibilities encompassed drafting and submitting comprehensive regulatory submissions to the FDA and international entities. Brooke's background also features significant involvement in surgical research at UC Davis, including a surgical research internship focused on animal preparation and anesthesia monitoring. Additional internships have included roles in clinical, regulatory, and quality functions at Dextera Surgical Inc., medical reimbursement at Silicon Valley TMS, and regulatory support at SI-BONE, Inc. Education was completed at the University of California, Davis, with a major in Biological Sciences emphasizing Neurobiology and Physiology.
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