Stephanie Allampalli

Stephanie has worked for almost 4 years in analytical development and 2 years in CMC regulatory affairs in the generic pharmaceutical industry before joining tranScrip in 2019 and has worked in regulatory affairs consultancy since.

Since joining tranScrip, Stephanie has worked on EU/UK MAAs and post-approval submissions with a focus on CMC aspects and  eCTD publishing. She also manages regulatory aspects of clinical trials in the EU/UK/Switzerland and conducts reviews of electronic Trial Master Files. Prior to moving on to regulatory affairs, Stephanie was involved in the analysis of immediate and sustained release oral solid dosage forms in support of assigned development projects in the generic pharmaceutical industry.

Stephanie holds a Bachelor of Science (honours) degree in Biology and Chemistry from the University of Malta.