Eva Vognild has many years of experience within the fields Drug Regulatory Affairs and Clinical Trials. Her main area of expertise is project management and guidance according to Norwegian and European regulatory procedures and requirements related to MAAs, variations, MA-transfers, renewals etc., incl. all aspects of the national phase of EU regulatory procedures.

She prepares or perform translations of all types of product related information, safety related documents, educational (RMP) materials, texts for the Norwegian Pharmaceutical Product Compendium etc.

She is also part of the Compliance Team, working with translations and review of marketing materials for medicinal products to ensure compliance with the Norwegian legislation and the guidelines from the Pharmaceutical Industry in Norway (LMI).