ERMS pricing
Discover the benefits of ERMS and get a quote!
Get a quote!
Ethical Review Management System| ERMS
eClinical tool for a streamlined process regarding study requests and the tracking of study portfolios.
ERMS provides the following benefits:
SUBMIT, REVIEW AND MANAGE STUDY PRTOCOLS IN JUST ONE DIGITAL ENVIRONMENT
- With ERMS the processes concerning the reviewing and managing of study requests will be designed and digitalized according to your own workflow.
- Generate multiple processes. This can be used to easily make a distinction between Medical Research Involving Human Subjects Act study requests, amendments, and progress reports.
- Through online meetings there can easily be communicated with applicants, head researchers, and MERC committee members.
- With Role Based Access Control different roles and rights can be set up.
- Let research protocols be easily and digitally reviewed by committee members of MERCs.
- With Contract & Document Management research protocols, amendments, and progress reports can be safely signed and locked.
- Link the ERMS tool with the CTMS tool and researchers can send the complete study protocol, amendments, and progress reports straight to the affiliated Medical Ethics Review Committees (MERCs).
GET AN OVERVIEW OF ALL RUNNING STUDIES
- MERC committee members quickly get insight in all statuses of running studies through study dashboards.
- Through Management dashboards all the information needed for inspections and year reports are directly available.
- Export all study related data to Excel (.cvs, xls), or other desired file types.
- Comply with 'Good Clinical Practice' principles: Audit Trail, Role Based Access Control, built-in SAE/SUSAR notifications, ISO27001 & NEN7510 certified and 21 cfr part 11 compliant.
- Let the ERMS easily communicate with applications, through an API.
