Multi-Site Software
Overview
Centralize
- Allow your IRB to manage research for both single site and multi-site studies, reducing research administration times and clarifying cooperative procedures
- Identify a Project Manager to serve as the Primary Principal Investigator for the multi-site study
- As the Primary Site, regulate the informed consent template to be used for all affiliate research sites
Collaborate
- Invite other site investigators to participate in multi-site clinical research using email notifications and home screen tasks
- Help ensure that regulations are met at all participating research sites
- Easily collaborate between multiple institutions or within departments at the same institution
- Allow coordinators at external sites to submit assurance statements electronically
Streamline
- Facilitate the process of multi-site collaboration, reducing study review and start-up times
- Centralize and track study documents from all affiliated sites
- Simplify the IRB review process while incorporating input from all sites
- Differentiate between submission forms specific either to the primary site or to other research sites
Government recommendations suggest that the use of a centralized IRB for NIH funded studies. Seamless collaboration can help to relieve IRB burdens, expedite the process of conducting multi-site trials, reduce work duplication, and cut expenses. Multi-Site Assistant from iMedRIS helps to create a consistent and efficient review process for any size research network.
