Investigator Handbook – Revised September 18, 2017

The Sterling IRB Investigator Handbook has been revised to include information regarding several topics including Sterling IRB’s policies and procedures related to e-consent, the recent FDA Guidance on waivers or alterations of informed consent for minimal risk clinical investigations, and Sterling IRB’s Board pre-review service. For a complete summary of changes to the Investigator Handbook, please see Page 2 of the Investigator Handbook or contact Sterling IRB at 1-888-636-1062 / This email address is being protected from spambots. You need JavaScript enabled to view it. for additional information.

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WHY CHOOSE STERLING?

Innovation. Passion. Commitment. We believe these are the essential components of strong teamwork.

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REVIEW BOARD

A diverse group of scientific and non-scientific members with nearly a century of collective IRB experience.

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RESEARCH IN CANADA

Sterling IRB has formed a strategic partnership with Veritas IRB.

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