The e-IRB Global is a complete web-based service for providing electronic solution for paperless documentation of Institutional Review Board (IRB) and its related activities. It also provides long term e-archival facility for IRB records as per regulatory agency requirements.
E-registration and login ID creation for individual IRB /sponsor/ CRO/ pharmaceutical company
One point details of registered IRBs for individual city/state/country
Login facility from anywhere/ any time with the help of unique ID and password
Login facility for individual IRB member for performing their relevant activities as assigned by IEC
Auto login ID creation/ modification/ deactivation and access rights management for individual user
Provision for uploading of clinical trial application for IRB review and approval of protocol/amendment(s)/ general documents/etc
Generation of different IRB records like Meeting Agenda, Minutes of Meeting (MoM), Decision Making, IRB Approval, etc
Provision for submission or reporting of study progress reports/ study updates/ study schedule/ SAE or AE management update/ Protocol Deviations
Provision for submission or reporting of study progress reports/ study updates/ study schedule/ SAE or AE management update/ Protocol Deviations
Tell us what you need and we will respond to your query within 24h!