Santa Barbara CA – Smarteeva announced the release if it’s Winter 2021 Post Market Surveillance Suite which will have enhancements to its Smart Complaint System, FDA MDR Reporting, EU MIR Reporting, and Recall Management. Some of these enhancements include, MDR QuickFill, EUMIR QuickFill, Faster Coding, Enhanced Audit Trail Management and many others.
“Our main focus, again, is R&D investment. We intend to become the premier Post Market Surveillance partner to Medical Device Companies” said Smarteeva CEO Plarent Ymeri. “In this release, the biggest focus was to make MDR and MIR completion faster and more accurate. Continuing our investments in ease of use and faster data collection, we added a new QuickFill search and copy capability which allows users to find similar MDRs and MIRs and instantly copy their contents.”
Recent FDA updates to the MDR Reporting Requirements have triggered a wave of upgrades to MDR implementations in Medical Device Companies. These updates are more than just cosmetic, they involve over 60 field changes, new codes and updated business rules.
As updates go, this was on a larger side and it affected companies large and small. This update and Smarteeva’s continued investment in R&D has led many companies to switch to a new and modern Post Market Surveillance Suite.
About Smarteeva:
https://smarteeva.com/
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 Salesforce.com Platform and utilizing the latest innovations in AI and Machine Learning, Smarteeva Software provides a true partner to it’s business users.
Media Contact Anita Rollo ****@smarteeva.com (805) 751-8767
