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Ms. Woodring joined Inspire in January 2000. As Senior Director, Regulatory Affairs, she is responsible for managing regulatory support for projects, including activities such as regulatory strategy, regulatory operations, safety reporting and project management. She received her Regulatory Affairs Certification in 2001. Ms. Woodring came to Inspire from Glaxo Wellcome where she spent six years in clinical research. There she participated in the submission of three NDAs for nine pulmonary drugs, and was instrumental in the design and execution of the asthma clinical trials performed to support the Advair NDA. Ms. Woodring completed her B.S. in Medical Technology at the University of Akron, and earned an M.S. in Pharmacy Administration from UNC - Chapel Hill. | 