Gain the BRANY IRB Advantage
Flexible and responsive to work the way you work
High standards for review quality and compliance
Owned by nationally recognized medical academic centers

 

BRANY IRB services & resources:
• IRB Committee
• IRB Administration
• Workflow Review & Recommendations
• Transfer of IRB Oversight
• Conflict of Interest
• Consent Requirements Review
• Notifications, Alerts and Reporting
• OneAegis for IRB Online Submission System
• Training

Ready for a new IRB experience?
Call BRANY IRB at 516-470-6979.

Establishing a new relationship with an Independent IRB may seem complicated. We help make it easy with an efficient, connected, and flexible approach.

Protocol Builder
Protocol Builder makes the process of writing, collaborating, and reviewing protocols faster and more efficient. A cloud-based solution, it can be customized to fit the protocol template and process needs of any IRB.

Informed Consent Builder
Informed Consent Builder provides an easier way to build, manage and generate
compliant informed consent forms A cloud-based solution, it can be customized for any consent form template and the process needs of any institution or IRB.

    Please provide us with more detail about your needs. Check all boxes that apply.

    Type of organization:
    Industry-sponsor or Company
    CRO
    Academic Institution, Academic Medical Center, Hospital or Healthcare System
    Independent Investigator/Researcher

    Study details:
    Biomedical study/trial for 1 to 4 sites
    Biomedical study/trial for 5+ sites
    Social Behavioral and Educational (SBER) study for 1 to 4 sites
    Social Behavioral and Educational (SBER) study for 5+ sites
    Single IRB (e.g. NIH funded multi-site study)
    Need an IRB budget for a grant-funded multi-site study
    Research requiring a Biosafety Committee (IBC)

    I am also interested in learning more about BRANY’s software solutions:
    OneAegis compliance management solution
    SMART CTMS
    Protocol Builder
    Informed Consent Builder