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 / info@sterlingirb.com for additional information.