Adam Tuszyner is Regulatory Compliance Specialist at Mabion S.A. With a strong background in clinical pharmacology and evidence-based medicine, Adam specializes in regulatory science and clinical development for biologic drugs. He has authored and co-developed a wide range of regulatory documents, including FDA and EMA briefing materials and responses to agency queries. His career highlights include participation in pivotal scientific advice with regulators and involvement in biosimilar drug approvals.