Laura Lind is a skilled regulatory affairs professional with extensive experience in the medical device industry. Currently serving as a Principal Regulatory Affairs Specialist and Regulatory Affairs Project Leader at Abbott since January 2025, Laura has a strong background in compliance and regulatory submissions. Previous roles include Principal RA Consultant at Fang Consulting Ltd, where comprehensive gap analyses of EU MDR were conducted, and regulatory support for US, EU, and global submissions. Laura held senior positions at Nonin Medical, Inc. and Covidien, specializing in patient monitoring systems and product submissions, alongside consulting roles focused on EU Technical File updates and regulatory compliance initiatives. Laura holds a Bachelor of Science degree in Nuclear Engineering from Iowa State University.
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