Sterling IRB
Sterling IRB is dedicated to providing expert guidance and personalized, high-quality institutional review board services. With over 30 years of experience, they focus on protecting the rights and welfare of research participants while ensuring regulatory compliance. They serve pharmaceutical and biotech companies, CROs, federal agencies, investigators, hospitals, and academic institutions, offering comprehensive IRB solutions across the board.
Industries
Nr. of Employees
small (1-50)
Sterling IRB
5500 Interstate North Parkway, Suite 515, Atlanta, GA 30328
Services
Ethics review and approval services for initial and continuing review of human subjects research, available as central and local review covering full board and expedited pathways.
24/7 secure portal for submission, retrieval, and management of study documents and forms to support sponsor, site, and institutional workflows.
Preparation and review of participant informed consent documents to meet regulatory and ethical standards.
Consultative service providing regulatory guidance on topics including eConsent, protocol modifications, IND/IDE responsibilities, emergency use authorizations, and Canadian regulations.
Certified translation of study and consent documents to support multi-language regulatory submissions and participant materials.
Training resources and education for investigators and site personnel on human subjects protection, compliance requirements, and study start-up processes.
Ethics review and approval services for initial and continuing review of human subjects research, available as central and local review covering full board and expedited pathways.
24/7 secure portal for submission, retrieval, and management of study documents and forms to support sponsor, site, and institutional workflows.
Preparation and review of participant informed consent documents to meet regulatory and ethical standards.
Consultative service providing regulatory guidance on topics including eConsent, protocol modifications, IND/IDE responsibilities, emergency use authorizations, and Canadian regulations.
Certified translation of study and consent documents to support multi-language regulatory submissions and participant materials.
Training resources and education for investigators and site personnel on human subjects protection, compliance requirements, and study start-up processes.
Expertise Areas
- IRB review and oversight
- Ethics review and human subjects protection
- Informed consent development
- Regulatory compliance and consulting (IND/IDE/EUA)
Key Technologies
- Secure web-based submission portals
- Electronic informed consent (eConsent)
- Automated submission and workflow systems
- Decentralized trial platforms and remote data-collection methods
News & Updates
Sterling IRB offices will be closed on May 26th in observance of Memorial Day.
Sterling IRB offices will close early on April 23rd in celebration of Administrative Professionals Day.
Sterling IRB offices will close early on April 23rd in celebration of Administrative Professionals Day.
Sterling IRB offices will be closed on May 26th in observance of Memorial Day.
Sterling IRB has been fully accredited by the AAHRPP since 2010.
Sterling IRB offices will be closed on May 26th in observance of Memorial Day.
Sterling IRB offices will close early on April 23rd in celebration of Administrative Professionals Day.
Sterling IRB offices will close early on April 23rd in celebration of Administrative Professionals Day.
Sterling IRB offices will be closed on May 26th in observance of Memorial Day.
Sterling IRB has been fully accredited by the AAHRPP since 2010.