EU Incident Reporting by Smarteeva

Smarteeva delivers state of the art simplicity with its newly released Manufacturer Incident Report for EU MDR

Smarteeva Post Market Surveillance and EU MDR Ready Suite

Smarteeva’s Postmarket Device Lifecycle suite of products provide an unsurpassed amount of efficiency with the ability to improve customer service and leverage the highest level of device utilization in the market.

Smarteeva Audit Trail – Quick Demo

Smarteeva’s Smart Audit Trail takes the record tracking to the next level of usability and productivity. With Smarteeva’s Smart Audit Trail organizations can quickly research and asses the state of their regulatory records. Say goodbye to hours of research to understand what transpired over time with your valuable data.

Smarteeva loves to partner with you

Reach out to us. Whether you are a Medical Device Company, a Healthcare organization we would love to talk to you.

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