Hummingbird IRB

Contact Information

Hummingbird IRB
197 1st Avenue

Suite 250
Needham, MA 02494
Phone: 1-855-447-2123
Email: info@HummingbirdIRB.com

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.

  • IRB Services for clinical trials Phase I - V
  • Specialty Boards
  • Consultative Services
  • Protocol development and pre-review
  • Daily Board meetings, capability for ad hoc meetings
  • Investigator Site Services
  • Project Management and a dedicated, single point of contact
  • Flexible pricing structure

Types of Research

  • Expeditable Research Review
  • Federally Funded Studies
  • Investigator Initiated
  • Institutional (academic, consortiums and collaborative)
  • Single and Multi-site review
  • Specialty Boards
    • Oncology
    • Respiratory
    • Central Nervous System
    • Rheumatology
    • Infectious Disease
    • Devices
    • Complimentary Alternative Medicine
    • Research on Incarcerated Individuals
    • Phase I
    • Innovative Study Design

Metrics

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.

  • Established in 2013
  • 15 Board members with an average of 10 years of experience in research and IRB review
  • FDA audit conducted in August 2013 with no findings
  • AAHRPP accreditation received in September 2014
  • Initial review turnaround time from receipt of a complete submission — 6 days
  • Study modifications and amendments processed within — 6 days

Sponsors/CROs

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

 

Contact Information

Hummingbird IRB
197 1st Avenue

Suite 250
Needham, MA 02494
Phone: 1-855-447-2123
Email: info@HummingbirdIRB.com

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