Seema is an experienced Regulatory professional who joined Quantum as a Regulatory Strategist. She brings over 11 years of progressive experience in clinical/regulatory development across multiple areas including oncology, paediatrics, cardiovascular, CNS, immunology, endocrinology, and infectious diseases. She is skilled in regulatory strategy and submissions across global markets including the EU (EMA), UK (MHRA), and US (FDA). Seema has demonstrated success in leading regulatory submissions from early-phase trials through to MAA and post-approval processes. She is also known for strong cross-functional collaboration, strategic thinking, and meticulous regulatory compliance. Seema has a BSc in Biomedical Science from King’s College London and a MSc in Clinical Drug Development from Queen Mary University of London.