📊 Last year, I worked on a project supporting the FDA registration of a medical device.
My task was to format clinical data tables and calculate general statistics based on a literature overview covering hundreds of published studies. The data was used to summarize safety and performance outcomes as part of the regulatory submission.
It was a detail-oriented project where accuracy and consistency were essential, and I appreciated the chance to contribute to something with practical, real-world implications.
Clinical data formatting and statistical analysis for FDA submission, based on a literature review of safety and performance in medical device studies.