Indre Larson is a seasoned Regulatory Affairs Consultant with extensive experience in the biopharmaceutical and medical device industries. Currently a Senior Regulatory Affairs Consultant at Vantage MedTech, Indre compiles regulatory submissions, implements quality management systems, and conducts audits. Previously, Indre held roles such as Director of Quality and Regulatory at Micron Medical Corporation and Regulatory Affairs Manager at Stimwave, where they managed quality systems and led compliance initiatives. Indre's background includes significant expertise in ISO standards, regulatory compliance, and quality assurance, underscoring their ability to drive complex projects effectively.
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