Georgia Quartey, PharmD
Global Patient Safety & Regulatory Affairs Fellow
Ironwood Pharmaceuticals

What is your current day-to-day role like at your company?

My current day-to-day role consists of attending various cross-functional meetings, both internally and externally, and collaborating on the authoring and maintenance of regulatory documents. The types of meetings I attend include global/regional labeling, maintenance of IND and/or NDA applications, regulatory strategy, regulatory intelligence, and regulatory operations. I also assist in the interpretation of FDA regulations and guidelines to ensure that published materials are compliant with the FDA.