Global Clinical and Pharmacovigilance Regulations MS

The Master of Science in Global Clinical and Pharmacovigilance Regulations in the School of Pharmacy at Temple University focuses on both disciplines of clinical trials and pharmacovigilance, enabling PharmD and MD graduates to pursue positions in U.S. and global clinicals trial projects, research administrators and safety directors in the global marketplace. This master’s program is part of the school’s regulatory affairs (RA) and quality assurance (QA) graduate program.

The curriculum provides the skills needed to manage and oversee clinical trials, supervise record-keeping, review clinical trial or post marketing safety data, and interpret results.