Tessa Vermeire is Senior CMC Writer at Ardena Ghent. She brings more than six years of experience in CMC writing, supporting pharmaceutical development programs with a strong focus on regulatory documentation.
Since joining Ardena, Tessa has contributed to the preparation of a broad range of regulatory documents, with particular expertise in Investigational Medicinal Product Dossiers (IMPDs) and Marketing Authorization Applications (MAAs). She is recognized for her structured approach, attention to detail, and ability to translate complex scientific data into clear and compliant regulatory documentation. At Ardena, she works closely with cross-functional teams to support the successful advancement of pharmaceutical development programs.
Tessa obtained her Master’s degree in Biomedical Sciences in 2013 and earned her PhD in Health Sciences in 2019. She has developed her pharmaceutical and regulatory expertise through hands-on experience across CMC documentation and regulatory support activities.
