Smarteeva releases its Winter 2020 Smart Complaint System to provide full EUMDR compliance for Medical Device Companies

Santa Barbara, CA – Oct 9, 2019 – Smarteeva announced the release if its Winter 2020 Smart Complaint System, which will have additional state-of-the-art enhancements to its Post Market Surveillance Suite. Some of these enhancements include:

 Full EUMDR post market surveillance capability
 Enhanced and record integrated smart decision trees
 Enhanced smart configuration capabilities and many more

Smarteeva pushes out new releases 3 times a year to coincide with the Salesforce Platform release schedule.

“We constantly take customer feedback and use it to enhance the capability of our offering,” said Smarteeva CEO, Plarent Ymeri. “In this release, the primary focus of our customers was EUMDR, and specifically, the MIR form and its integration with Risk Management. Also, we wanted to make our implementations a lot faster, so we invested a significant effort in our smart configuration capabilities. Now, most business rules can be configured from 1 screen and in a very intuitive way.”

About Smarteeva:

Based out of Santa Barbara, CA, Smarteeva Software provides cutting edge and innovative Post Market Surveillance applications for the Medical Device industry. Smarteeva’s Complaint Handling, Adverse Event Reporting, Risk Management and Recall Management solutions prioritize compliance, organizational efficiencies and user friendliness. Built on the Platform and utilizing the latest innovations in AI and Machine Learning, Smarteeva Software is a tangible partner to its business users.