A bit about me
Leveraging her background as a pharmacist, Sabrina is committed to supporting clients in navigating the complex regulatory environment at both BeNeLux and European levels.
Career highlights
Sabrina joined the Kintiga team in January 2023 and brings experience in regulatory affairs and pharmacovigilance across the BeNeLux region and global markets. She has managed end-to-end regulatory activities, including pre- and post-authorisation processes, and contributed to pharmacovigilance as deputy local contact, performing local literature screening and Risk Management Plan (RMP) writing.
Sabrina’s expertise also includes drafting reimbursement dossiers, medical information, and designing e-learning solutions to support compliance and training.
Her strong analytical skills and detail-oriented approach are complemented by hands-on experience in regulatory submissions and safety processes, making her a valuable asset in ensuring compliance and facilitating market access.
Expertise
- Management of all local (BeNeLux) and global regulatory affairs activities (pre- and post-authorisation)
- Pharmacovigilance activities (deputy local contact person, local literature screening, RMP writing, etc.)
- Writing clinical part of reimbursement dossiers
- Medical information
- Design and implementation of e-learnings
Personal interests
Outside of work, Sabrina enjoys spending quality time with her family, especially her two young children who keep her happily busy. When time allows, she enjoys working out at the gym.
