
Jeanne C.
Director Global Regulatory Affairs @ Kite Pharma
United States
Greater Philadelphia
Pharmaceuticals
Regulatory Affairs, CMC Regulatory Affairs, Regulatory Submissions, FDA, Biotechnology, Biopharmaceuticals, Pharmaceutical Industry, Change Management, Quality Assurance, Manufacturing, Validation, GMP, GxP, SOP, 21 CFR Part 11, CAPA, Technology Transfer
Experience
Sr. Scientist, Chemistry, Manufacturing & Control
Overland Park, Kansas
Cardinal Health Specialty Solutions partners with healthcare providers and pharmaceutical manufacturers to ensure patients have access to the therapies they need, when they need them. From supporting manufacturers on the path to successful product approval, commercialization and optimization, to delivering the products providers need and the efficiencies they want, we use our experience and expertise to improve specialty care. The Regulatory Sciences group of Cardinal Health Specialty Solutions partners with global pharmaceutical, biotechnology and medical device companies to solve complex regulatory challenges. Our technical consultants, through industry and FDA training, provide regulatory and product development consulting services at all phases of development in order to help companies ensure compliance with global regulatory agencies. Our regulatory strategies and services are designed to allow companies to expedite the development process, achieve regulatory approval and keep approved products on the market. Views shared through LinkedIn are my own and may not be representative of the views of my employer.
Jeanne C.'s Contact Information
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