SciLucent’s staff includes scientific, medical, and regulatory professionals with expertise and experience in all aspects of healthcare product development and marketed product support.
Gillian A. Miller, Ph.D., RAC (EU, US)
Regulatory Strategy, Documentation, and Implementation; Nonclinical and Clinical Development and Implementation; Project Management
Gillian Miller is an expert in the development of nonclinical and clinical programs to further drug development. She has played an integral role within project teams guiding investigational new drugs, biologics, and approved drugs through regulatory and clinical processes in the U.S., Europe, and Canada. She has authored orphan drug designation requests for submission to FDA and EMEA, prepared INDs, drafted SOPs, and represented sponsors at FDA meetings. Gillian's therapeutic areas of expertise include oncology, gastroenterology, stroke, and neurology.
