We are a partner in all phases of a market entry; from initial thought partnership to broad market analyses, defining a market entry strategy as well as implementation, including setting up a local organization or securing efficient implementation of defined strategies and tactics to reach your market objectives.
Nordic Head of Regulatory Affairs+45 3590 1129margrethe.andersen@pharmarelations.dkWith 25 years of experience in the pharmaceutical industry, Margrethe is a science-driven Regulatory Affairs expert with deep expertise across the product life cycle - from early clinical stages to life cycle management. Specializing in pre-approval activities for small and mid-sized pharmaceutical companies, Margrethe has collaborated with regulatory authorities across Europe, the US, and Japan. Additionally, she has experience with generics and brings 9 years of expertise in CMC. Her strong project management and leadership skills make her a valuable asset in regulatory strategy and execution.
Beyond her industry role, Margrethe shares her knowledge as a lecturer at Atrium, a leading life science course provider that collaborates with the University of Copenhagen.
If you have any questions, please feel free to contact Margrethe directly
- she will be happy to help you.
