
In the first part of a two-part interview, Paz Vellanki of Precision for Medicine explains what sponsors should bring to early FDA meetings and how manufacturing and assay readiness can delay rare disease trials.
A leading global pharmaceutical company needed to find new ways to help scientists focus more time and attention on innovation and strategic drug projects. Medium-complexity tasks, such as maintaining cell lines, performing QC assays, and conducting routine chromatography work, were outsourced, allowing scientists to focus on their core research while improving overall efficiency.






