eIRB

Features eIRB

E-registration and login ID creation for individual IRB /sponsor/ CRO/ pharmaceutical companyOne point details of registered IECs for individual city/state/countryLogin facility from anywhere/ any time with the help of unique ID and passwordLogin facility for individual IRB member for performing their relevant activities as assigned by IRBAuto login ID creation/ modification/ deactivation and access rights management for individual userProvision 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 DeviationsEmail/SMS intimation for uploading of application, acceptance of application, updates, request, meeting schedule, decision making, training schedule, etc.Generation and maintenance of individual IRB member’s CV/ IRB SOPsOne click availability of different type of reports related to application/ update/ request/ IRB member training / IRB decision making/ IRB composition/ IRB member CV/ IRB member job responsibility / etc.Archival and periodic backup of all records including superseded documents for required time period.At e-IRB Global, we accept every challenge as an opportunity to be solved creatively to provide effective solutions for related services.
We believe that, every service that we provide will supports to our customers in term of speed, quality, reliability and accountability of related works.Our philosophy is to satisfy the customer and give him worth of every penny they spend on us.
If you have any enquiry, we would be happy to hear from you.