Catherine Parker

Catherine has over 20 years’ experience working in the pharmaceutical industry, specifically in the area of Regulatory Affairs.

During her career, she has worked across clinical trials, OTC products, generic products and innovator products, and has broad experience in post-marketing procedures, manufacturing, supply chain activities and lifecycle management of products approved both in Europe and worldwide. Catherine has spent over nine years working in Australia and New Zealand, giving her strong knowledge of global regulatory requirements and procedures. She also has a good working knowledge of vaccine labelling requirements in Europe and the UK. 

Catherine has worked for several large generic and innovator pharmaceutical companies and has additional experience working within a large multinational CRO.