Louise Spencer

With over two decades of experience in regulatory affairs, Louise is a Senior Regulatory Affairs Manager with a deep expertise in human medicinal products. Since 2001, she has navigated the complexities of pre-submission activities, marketing authorisation applications, and the upkeep of product portfolios for both centralised and national products. Her proficiency extends to providing clinical trial regulatory support and adept project management.

Louise’s versatile career includes significant contributions to veterinary medicinal products, showcasing her adaptability and broad knowledge base. She has excelled both as a regulatory consultant and within a small pharmaceutical development company, bringing a wealth of practical insights and strategic vision to her roles.