Senior Director, Regulatory and Quality Assurance @ From May 2015 to Present (8 months) Director, Regulatory Affairs @ From July 2002 to Present (13 years 6 months)
Shelley Mendenhall is skilled in: Regulatory Submissions, FDA, Clinical Development, GMP, Pharmaceutical Industry, Regulatory Affairs, Biopharmaceuticals, CRO, Drug Development, SOP, Biotechnology, Life Sciences, Clinical Trials, Oncology, Drug Discovery