Thorough expertise, compliant considerations, accurate documentation and dependable service are expectations for the oversight of a clinical trial and are shared responsibilities for safe-guarding the research participant.

HIRB recognizes the importance of scientific constraints, challenges of urgency, required adherence to quality and sensitivity to cost in conduct of clinical research must balanced with the most critical component, risk management for the research subject as well as the sponsor. As a partner in the advancement in science and medicine, HIRB balances business imperatives while ensuring the ethical protection of the subjects participating in a study.

Hummingbird IRB experienced team provides:

  • Flexible Pricing
  • Pre-review
  • Regulatory Guidance
  • Daily Meetings
  • Single Point of Contact and Project Management Oversight
  • Consultative Services