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Alpha IRB features the following services: How often does Alpha IRB meet? Alpha IRB has board meetings every Monday and Wednesday Protocol submissions are due 4 business days prior to review Site submissions are due 4 business days prior to review Expedited items are reviewed daily When are approval documents sent to the sites? Approval documents are available the day following approval through our OASIS IRB Manager Web Portal Documents may be shipped hard copy if desired within 48 hours of approval Does Alpha IRB have a web portal available for Phase I-IV studies? YES - Alpha IRB has implemented OASIS - the IRB Manager Web Portal system What does OASIS mean to my study? Ability to track the progress of a study or site submission through Alpha IRB review process Sponsor and Site information captured so repeat information will NOT have to be typed new for every study All submission and IRB documents available online No more paying for shipping fees and document request fees Efficiency Approval documents for amendments can be completed expeditiously no matter how many sites are in the study Sites may make all document submissions electronically Does Alpha IRB utilize our own standard ICF template language for each study Consent Form? You may submit your template ICF as prepared within your company What is Alpha IRB practice regarding prices and price quotes? Alpha IRB is happy to sign Service Agreements with Sponsors to allow for consistent pricing across all studies Alpha IRB will maintain the agreed prices throughout the life of the study Will I have one contact for my study? YES - our OASIS web portal allows our study management specialist to have a direct relationship with your study team from start-up to close out. Is Alpha IRB registered with the Office for Human Research Protections (OHRP)? Yes, Alpha IRB’s OHRP Registration Number is IRB00006205.

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