Kim Gaumer

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Vice President, Regulatory Affairs and Quality Assurance

Ms. Gaumer has served as vice president, regulatory affairs and quality assurance since 2012.

Ms. Gaumer has over 20 years of US and European regulatory affairs and quality experience, covering both drug and drug-device product candidates. Prior to joining AcelRx she spent three years at Zosano Pharmaceuticals, Inc., a drug delivery company spun out of Johnson & Johnson, where she was vice president, regulatory affairs and quality assurance, focused on establishing and leading their regulatory, quality assurance and quality control organizations.

Prior to Zosano, Ms. Gaumer held positions of increasing regulatory responsibility at ALZA Corporation, a Johnson & Johnson company, most recently serving as senior director, regulatory affairs. At ALZA, Ms. Gaumer provided regulatory supervision for several development programs through Phase 3B including both New Drug Application and Marketing Authorization Application experiences. She holds a Bachelor of Arts in human biology from Stanford University..