Smarteeva’s functionality transforms PMS reporting by automating the entire process, from data preparation to final report submission. The platform’s ability to aggregate data from multiple sources, manage templates, and automate text generation significantly reduces manual effort and improves the accuracy of regulatory submissions.
With its built-in notifications, section assignments, and finalization workflows, Smarteeva ensures that every aspect of PMS reporting is handled efficiently and on time. Smarteeva’s project workflow not only boosts productivity but also enhances compliance by making PMS reporting simple, transparent, and fully automated.
About Smarteeva
About Smarteeva: Headquartered in Southlake, Texas, Smarteeva Software pioneers Post Market Surveillance for the medical device sector. We offer Complaint Handling, Adverse Event Reporting, Risk Management, and Recall Management solutions, designed for compliance and streamlined operations. Built on Salesforce.com with cutting-edge AI and Machine Learning, we are true partners to our users.
Reach us at: info@smarteeva.com | www.smarteeva.com
