Anusha Foy, BSc, LLB, is responsible for leading IQVIA Biotech Clinical Solutions’ global regulatory affairs department.
She oversees regulatory clinical research projects, safety reporting for customers, and provides the project team with guidance, training and strategic planning.
Ms. Foy has more than 15 years of regulatory affairs experience globally across many therapeutic areas including oncology, CNS and respiratory research. Ms. Foy’s previous experience includes senior regulatory affairs roles at a variety of organizations including the Medicines and Healthcare products Regulatory Agency (MHRA) and two global CROs.
She holds a BSc in Medicinal Chemistry from University College London; a Bachelor of Law from Birkbeck College London and qualified as a non-practicing Barrister in England and Wales.