Sara Mohamed Mahmoud

Completed a summer internship at Viatris as part of my Master’s in Pharmaceutical Sciences at UCLouvain. Acquired a better understanding of Pharmacovigilance, Regulatory Affairs, Medical Affairs, and Quality, learning about cross-department collaboration and the importance of patient safety.

Administrative support during the transition from the European Clinical Trials Directive to the European Clinical Trials Regulation within the R&D division

Exposure to different departments of the pharmaceutical industry, including Production, Quality Control, Quality Assurance, and Technical Management