Automated Trial Monitoring Workflows Make Small Teams More Efficient

Enterin has been working to improve the medical community’s understanding of the link between infections, dysfunction of the enteric nervous system (ENS) of the gut, and the early onset and chronic progression of neurodegenerative disease. The small pharmaceutical therapy developer’s long-term mission is to become the world leader in creating therapeutics that repair the gut-brain axis.

Until 2019, Enterin’s clinical monitoring team was manually creating reports, confirmation letters, and follow-up letters. “Generating the letters and reports was cumbersome, and took 5-6 hours a week away from site monitoring,” said Senior Manager for Clinical Monitoring Lisa Lutz. To increase efficiency, Enterin wanted to automate the generation of letters and reports, automatically notify clinical research associates (CRAs) and other stakeholders when site visits were due, and make it easier to share data with senior leadership and site managers.

See what happened when Enterin streamlined its clinical monitoring workflow with Medidata Rave CTMS (Clinical Trial Management System), a cloud-based solution for end-to-end trial management.