Since I started my career in Regulatory Affairs CMC for one of the world’s top 5 pharmaceutical companies in 2001, I have been involved in new registrations and post-approval activities for Biotech products worldwide, including intensive collaboration with colleagues in Japan and USA. Since I joined Starodub in December 2016, I have further expanded my knowledge working on projects for Biotech (e.g. recombinant proteins, antibody drug conjugates, vaccines), Small Molecules and Medical Devices for several small and large companies, including development and post-approval activities. I have also been involved in development, improvement and implementation of different business systems. Furthermore, I have developed my personal skills in leadership, problem solving, communication and priority setting. Apart from being a valued expert in Regulatory Affairs CMC by colleagues all over the world, I have also learned a lot about Quality, Compliance and Improvement projects. The Starodub team consists of a group of very experienced people in various areas of Regulatory Affairs, who are dedicated to perform their tasks in a professional and efficient way. I am proud to be part of this team and to be able to contribute to further development of the company, especially in Biotech.