Linde De Grande is Senior CMC Writer at Ardena. She brings 8 years of experience supporting pharmaceutical and biotech companies across drug product development and regulatory documentation within GMP-regulated environments.
At Ardena, Linde focuses on developing clear and high-quality CMC documentation and supporting cross-functional teams across tech transfer, process validation, and lifecycle management activities. She is recognized for her structured approach and her ability to translate complex scientific and technical data into compliant regulatory documentation.
Linde obtained her Master’s degree in Biomedical Sciences and earned her PhD in Pharmaceutical Sciences from Ghent University.
