Hannah Wiborg

Hannah is experienced in advising on European and German regulatory law, covering the entire life cycle of a product, e.g., clinical research and development, manufacturing and marketing authorization, reimbursement and commercialization. Her expertise further covers the review, revision and drafting of commercial agreements, such as complex manufacturing and supply agreements, license agreements, service agreements with HCP and healthcare institutions, contracts with health insurance companies or general terms and conditions. Further key aspects of her work are healthcare compliance and advertising, innovative medicinal products/ATMP and orphan drugs, (online) pharmacies and platforms, and the use of AI in the healthcare industry.

Hannah had her first contact with health care law during her studies. After her First State Exam, she worked in a law firm in Berlin specializing in medical law. During her legal clerkship she worked in the legal department of the Charité hospital and in a boutique law firm for health care law.