Company Profile
Our Mission
To protect the rights and welfare of research participants by ensuring that the risks never outweigh the value of human life.
Our Profile
Liberty IRB, Inc. is an independent institutional review board (IRB) located in DeLand, Florida. With the ability to review Phase I-IV pharmaceutical, device, biologic, behavioral and psycho-social research. Liberty IRB strives to produce timely, diligent reviews of clinical research. Liberty IRB is also a member and on the executive board of the Consortium of Independent Review Boards (CIRB) which meets with government regulators on issues for the protection of research participants. Liberty IRB was granted full AAHRPP accreditation in 2009. Liberty is registered with OHRP and FDA as IRB00003411 and is in compliance with all federal regulations.
Benefits
- Liberty IRB is comprised of diverse members who collectively represent a wealth of experience and expertise. Scientific, ethical, community and administrative perspectives are represented and integrated into the application of ethical research concepts.
- IRB members receive initial and ongoing education in the protection of human subject rights.
- Liberty IRB has incorporated a specialized database to ensure compliance with regulations and to facilitate timely reviews of submitted materials. This database also contains extensive query abilities.
- Bi-weekly scheduled IRB meetings and efficient processing of time sensitive documents provide rapid turn around of study materials presented for review. Study document turnaround following a meeting is 2 business days.
- FDA compliant
- User friendly IRB application and submission process
- Pre-Review of submission documents
Services Available
- Multi-institutional review of clinical research with project management approach and excellent communication to individual sites and sponsors.
- Subject informed consent preparation and translation services.
- Good Clinical Practice (GCP) audits of investigator practices, Contract Research Organizations, IRBs and regulatory consultations.
- Customized Investigator training, CRA training, and CRC training available.
Multi-Center Trials
- Project Management approach to reviews which enable you to speak to one primary contact that is responsible for your study.
- Comprehensive database enables efficient tracking of studies as they are processed throughout the system.
- Excellent communication to the sites directly involved in the research
- Assistance with regulatory packet preparation and form completion prior to site distribution.
- Streamlined processing of amendments, consent revisions and unanticipated problem notifications
- Competitive Pricing.
- Copies of regulatory documents provided, at your request, to CROs and sponsors.
- Secure portal allows you access to information on all sites.
