Your Comprehensive Solution for everything in Post-Market Surveillance, AI & Innovation

Your Comprehensive Solution for everything in Post-Market Surveillance, AI & Innovation

Dear Readers,?

I'm Plarent, CEO of Smarteeva, and I'm thrilled to welcome you aboard the first edition of the Smarteeva Pulse, your monthly dose of news and solutions in the Post-Market Surveillance world.

The medical device landscape is a dynamic ecosystem, constantly buzzing with new regulations, technological advancements, and industry trends. Keeping pace and adapting quickly are crucial for success, but staying informed can feel overwhelming.

That's where Smarteeva Smart Pulse comes in.

Subscribe to get your monthly updates on the Medical Device Industry.


About Us:

Smarteeva offers a suite of salesforce packages that help medical device companies automate critical post-market management functions. By seamlessly integrating with Salesforce Service, Sales, Experience, and Analytics Clouds, our platform goes beyond traditional complaint management, providing advanced features like AI-powered analytics, automated workflows, and regulatory compliance tools. Smarteeva's integration with Salesforce Service Cloud ensures a smooth transition from initial customer interaction to comprehensive complaint management.

This holistic approach empowers medical device manufacturers to Enhance customer experience, Mitigate risks, Optimize operations and Ensure compliance.

Know More


Dreamforce x Smarteeva

Smarteeva at Dreamforce by Salesforce

Join the Smarteeva team at Dreamforce for an enlightening experience! Discover how our innovative solutions empower medical device companies in the Salesforce ecosystem. Don't miss this golden opportunity from September 17-19 in San Francisco, CA to learn, innovate, and connect with global industry trailblazers and Salesforce enthusiasts.

Register Now


Customer Spotlight

A Customer Case Study

A Leading global medical technology required a robust Recall Management system that could handle multiple Recalls, Global Affiliates, Letter Translations, Notifications, and Feedback Collection. Read how the company manages Recalls with Smarteeva’s Post-Market Platform.

Download Case Study


Industry News


Image Credit: Shutterstock

The FDA has released a framework outlining its coordinated approach to regulating AI in medical products. This collaborative effort across different agency centers aims to protect public health while fostering responsible AI innovation.?

Download Paper



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