E&I is dedicated to the ethical protection of human subjects in research and is experienced in the review all types of clinical and non-clinical research conducted in institutional settings, or in private practices all over the United States and Puerto Rico.

Over the past 25 years our boards have developed expertise in the following areas:

Clinical Trials

  • Phase I research
  • Phase II and III clinical trials
  • Post marketing / Phase IV clinical trials
  • Device studies
  • HUD and HDE Devices
  • Orphan Products
  • Expanded access clinical trials
  • Multi-center clinical trials (currently up to 1800 sites)
  • Repositories
  • Diagnostic Testing

Non-invasive / Non-clinical research (Social, behavioral and educational studies)

  • Survey trials
  • Health outcome-based trials
  • Registry studies
  • Educational / School based research
  • Grant Reviews

Additionally, the E&I administration offers consulting services to assist in developing institutional review boards, training and education services, auditing and monitoring and protocol development.