Dr. Terblanche is the Senior Business Process Consultant at VECTOR Life Sciences. She holds a Ph.D. in Cardiovascular Physiology from North-West University, with multiple peer-reviewed publications. During her doctoral studies, she developed a keen interest in regulatory affairs, which has since become her career focus. With a decade of experience in regulatory processes, Dr. Terblanche specializes in compiling eCTD submissions, with expertise in both the technical and scientific dimensions of pharmaceutical submissions. She has also co-authored eCTD specifications and procedures, providing critical regulatory insights across several African countries. Her work includes implementing RIMS solutions in these regions, including in one country that has utilized eCTD for over ten years, with a recent update to its framework. Her industry experience from one of South Africa’s top 15 pharmaceutical companies uniquely positions her to guide RIMS implementations with a deep understanding of industry needs and regulatory requirements.