Eeva-Maija has worked in the pharmaceutical industry for nearly 20 years and brings with her a wealth of drug development experience. Her experience ranges across all aspects of drug development, including early phase formulation, scale up, commercialisation, quality control, marketing authorisation applications, technology transfers and commercial product maintenance. She has thorough knowledge of sterile product manufacturing techniques and regulatory requirements. Welcome to Medfiles Eeva-Maija!
Eeva-Maija and our pharmaceutical chemical expert team are here to help you. Whether you are in need of a wholly new marketing authorisation, a single variation to maintain your marketing authorisation or strategic consultancy, you can trust us to take care of it for you. We will guide you through regulatory submissions by planning applicable development studies and the documentation needed to meet the regulatory requirements.
Please contact Regulatory Affairs Director Minna Haapalahti for more information about our services.