Advarra eRegulatory Management System allows you to route documents to staff and notify them automatically when new documents are available. 

With this system,

    • Documents can be uploaded, searched, updated and signed electronically.
    • Standard templates can be created and customized for each study type.
    • Staff credentials can be shared across multiple protocols.
    • PIs can delegate tasks at the system level to reduce the time needed to route documents.
    • Protocol documents for investigator-initiated multi-site trials can be managed efficiently.

Training & Support Documents

Standard Operating Procedures