Linda McBride brings significant expertise in preparing teams for successful interactions with health authorities and for delivering approvals for marketing applications, while striving to achieve the corporate vision for success based on her more than 35-year career in the pharmaceutical industry. She has directed the regulatory efforts for 300+ clinical trials conducted worldwide for small molecules, biologics and combination products and led numerous global marketing applications for anti-infective, cardiorenal, dermatology, neurology, oncology and pulmonology products. Linda earned her B.S. in Pharmacy at the University of Missouri, is a registered pharmacist and has obtained a regulatory affairs certification from RAPS.
