Midlands IRB supports the advancement of science and medicine by safeguarding the rights, health, and well-being of human research participants. We are committed to the efficient and ethical conduct of clinical trials, and serve our clients with:

  • Quality and Timely Review
  • Personalized One-on-One Service
  • Single and Multi-Site Reviews
  • Twice Weekly Board Meetings
  • Informed Consent Development
  • Education and Training Services
  • Certified Translation Services
  • Prompt Turn-Around
  • 24/7 Secure Web Portal
  • AAHRPP-Accredited
  • Clear FDA Audit History
  • Diverse Board Rosters
  • All Phases of Research in All Therapeutic Areas
  • Extensive Phase I Experience
  • Device Studies
  • Biologic Studies