Strong Regulatory Compliance Sterling IRB holds full AAHRPP accreditation and offers comprehensive review services in the US and Canada, highlighting its commitment to high standards in human subject protection. This positions the company as a trusted partner for pharma and biotech organizations seeking reliable IRB services.

Efficient Approval Processes With protocol reviews within five business days and site review turnaround within 24 hours, Sterling IRB demonstrates a focus on speed and responsiveness, which can appeal to sponsors and CROs needing quick regulatory approvals to accelerate clinical trials.

Technology-Enabled Service Utilizing advanced web portal solutions like SilverLink and employing modern tech stacks including HTTP/3 and Nginx, Sterling IRB emphasizes secure, fast document management, making it attractive for clients prioritizing efficient, tech-driven regulatory processes.

Responsive Customer Support The dedicated CIP Certified account managers providing a single point of contact suggest a personalized service approach, reducing client management complexities and fostering long-term relationships with research organizations.

Growth and Market Position With revenues between 10 and 25 million dollars and a dedicated focus on safeguarding research participants, Sterling IRB is well-positioned to expand its client base among mid-sized research organizations and sponsors looking for high-quality IRB partnerships.