Salus IRB
Non-profit, AAHRPP-accredited institutional review board providing ethical review and regulatory oversight for human subjects research. Offers single-site, central (single) IRB and international review services, review of phase I–IV clinical trials and social, behavioral and educational research, exemption assessments for minimal-risk studies, and consultative support for sponsors, institutions, and investigators.
Industries
Nr. of Employees
small (1-50)
Services
Ethical and regulatory review for single-site studies, multi-site studies using a single/central IRB model, and international research.
Assessment of minimal-risk research to determine eligibility for IRB exemption.
Advisory support for research ethics, protocol submission processes, and compliance matters.
Ethical and regulatory review for single-site studies, multi-site studies using a single/central IRB model, and international research.
Assessment of minimal-risk research to determine eligibility for IRB exemption.
Advisory support for research ethics, protocol submission processes, and compliance matters.
Expertise Areas
- IRB review and human subjects protection
- Single-IRB/central IRB operations
- International ethical review
- Oncology research ethics
Key Technologies
- IRB management systems
- Centralized (single) IRB review model
- Remote and international ethical review processes
- Regulatory accreditation and compliance frameworks
News & Updates
The parent clinical trials team attends conferences and events throughout the year to present and engage with the research community.
Maintains accreditation from an established human research protection accreditation body.
The parent clinical trials team attends conferences and events throughout the year to present and engage with the research community.
Maintains accreditation from an established human research protection accreditation body.