Ms. LeBlanc is a quality and compliance professional with 36 years of experience in pharmaceutical drug development. She has effectively led a global Quality organization supporting the development and commercialization of new products, including supply of materials for the clinical trial program, and life cycle management of existing products. Her extensive experience also includes development and implementation of Quality Management Systems governing drug development activities within a Good Manufacturing Practices environment. She has a broad knowledge of pharmaceutical development and the expertise to lead and collaborate for the effective commercialization of quality pharmaceutical products.
Expertise