Clinical Research Management Office

CRMO Home | Services & Fees | Educational Resources | Publications | Schedule

Services
  • Maintenance of regulatory documents,
  • Keeping lab normals and certificates,
  • IRB member list,
  • Processing of all serious adverse events to IRB,
  • Processing amendments to IRB,
  • Submission of annual updates to IRB,
  • Keeping current versions of consent form and protocol on Lombardi website