Facey's research team includes highly trained and motivated investigators and clinical research coordinators. Our entire research staff has been involved with extensive initial and ongoing training (in class, on-site, and web-based). Our training focuses on the following areas:
  • Good Clinical Practices (GCPs)
  • Informed consent / human subject protection
  • Clinical research regulations including 1572 requirements
  • Drug accountability
  • Composition of the research industry and drug development process
  • Patient recruitment and retention
  • Study conduct (from IRB submission to site close out)
  • HIPAA and its implications in the research arena