Louise is a Regulatory Affairs and Pharmacovigilance expert and has worked in the industry for over 17 years. Her expertise covers all phases of product lifecycle, from clinical development through to marketing authorization, and post-approval activities.
Throughout her career she has gained experience in the area of biologicals, ATMPs and new chemical entities. Louise holds a Ph.D. in molecular science from the Institute for Toxicology, Johannes Gutenberg-Universität, Germany. She has a Masters in drug design and biomedical science and an honours degree in toxicology.
Louise is in charge of tranScrip’s Dublin office, and manages a team of regulatory professionals in the areas of pharmaceuticals and medical devices.
Louise is also a member of both the TOPRA and RAPS regulatory associations.
We are always interested to hear from experienced professionals that are looking to develop their career with tranScrip.View all vacancies
We have teams of life science and R&D experts to help achieve your goals and seize opportunities. Whatever your project requires, we have the people to meet your needs.