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Peggy Hansen

General Manager Contract Development & Manufacturing and Sr VP Regulatory & Clinical Affairs at Regenity Biosciences

Peggy Hansen has a wealth of experience in the pharmaceutical and medical industries. Peggy began their career as a Quality Assurance Engineer and Regulatory Affairs professional at ReGen Biologics from 1991 to 1995. Following this, they worked as a Clinical and Regulatory Affairs Consultant at ReGen Biologics from 1995 to 1996.

In 1996, Peggy joined 3M as a Senior Regulatory Affairs Associate, where they worked until 2000. Peggy then moved to Surmodics and held the position of Regulatory Affairs Manager for one year.

From 2001 to 2009, Peggy worked at Collagen Matrix, Inc., where they started as a Sr. Director of Clinical, Regulatory Affairs, and Quality Assurance. Peggy then advanced to Vice President, overseeing Clinical, Regulatory, Quality Assurance, and Marketing. In 2016, they were promoted to the role of Senior Vice President of Quality and Regulatory Affairs. Most recently, Peggy has been the General Manager of Contract Development & Manufacturing and Senior Vice President of Regulatory & Clinical Affairs at Collagen Matrix, Inc., a position they have held since March 2020.

Peggy's extensive experience and senior roles in quality assurance, regulatory affairs, clinical affairs, and marketing make their a highly skilled and valuable professional in the industry.

Peggy Hansen attended Cornell University from 1987 to 1991. No specific degree or field of study was mentioned.

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Timeline

  • General Manager Contract Development & Manufacturing and Sr VP Regulatory & Clinical Affairs

    March, 2020 - present

  • Senior Vice President, Quality and Regulatory Affairs

    June, 2016

  • Vice President, Clinical, Regulatory, QA, and Marketing

    October, 2009

  • Sr. Director, Clinical, RA, QA

    October, 2001

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