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Beverly Hanson

Compliance Analyst, Mayo Clinic

As a member of the Manufacturing Compliance Office within the Integrity and Compliance Office, Beverly supports manufacturing teams at Mayo Clinic with product lines ranging from stem cells to artificial intelligence. She also supports a GLP program in Radiology Research. She collaborates with the teams to build their new programs to meet the federal regulations and conducts compliance monitoring for active product lines.

Previous to her Mayo Clinic work she was a scientist in pharmaceutical research at Parke-Davis in Ann Arbor, Mich. She has been at Mayo Clinic for twenty years where she has held various quality and regulatory roles within software quality assurance, clinical trials operations, clinical laboratory accreditation and compliance, and currently with FDA-regulated manufacturing compliance.  She has a BS in Biology from the University of Minnesota, Duluth and a BS in Chemistry from the University of Wisconsin, River Falls.