Tim Chesworth

Global Head Medical Device Regulatory Affairs @诺华

GB

Lead the Regulatory Affairs Device group within Novartis Regulatory Affairs• Accountable for the development and implementation of the regulatory strategy for all Novartis Medical Devices, Device components of Combination Products and Software-as-Medical Device for all therapeutic areas including Ophthalmology, Respiratory/Allergy, Neuroscience, Cardiovascular/Renal/Metabolism, Immunology/Hepatology/Dermatology, Oncology and HaematologyResponsible for developing and implementing regulatory strategies and processes for both new and existing medical devices and combination products.• Provide Medical Device regulatory interface with senior management• Monitor changes in the global regulatory Medical Device environment and oversee process for incorporation of emerging trends into internal regulatory strategies• Play an active role in leading and shaping Medical Device regulatory policy development via industry groups and directly with regulatory agencies

Newcastle University

BSc (Hons), Chemistry