Ginger Emrich is a senior regulatory affairs professional with over twenty years of experience in the medical device and in-vitro diagnostic industry. They have extensive knowledge of US and international regulations, emphasizing new device registrations and change control processes. Ginger’s career includes roles at Abbott Laboratories and Roche, where they contributed to quality assurance, complaint handling, and regulatory affairs. They hold a Bachelor of Science in Biology from Purdue University, awarded in 2002.
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