Developed and staffed by respected members of the IRB community with specialized expertise in medical, ethical and regulatory matters, Hummingbird IRB provides independent central IRB services for institutional and commercial clients.
Though not the largest IRB, Hummingbird IRB fully intends to be the best and although new as an entity, its members are highly seasoned and respected members of the IRB community. Knowing how important rapid turnaround is to the overall progress of a study from the site and sponsor perspective, Hummingbird has developed modern, forward thinking SOPs and is creating unique and easy to use software.
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: