
Smarteeva is a provider of advanced post-market surveillance solutions for medical device companies, leveraging artificial intelligence (AI) and machine learning to streamline operations and enhance regulatory compliance. Their product suite includes Complaints Management, Recall Management, Adverse Events tracking, and MDREngine, which aggregates medical device regulatory data. Smarteeva's solutions aim to improve customer service, operational efficiency, and patient safety by automating complaint handling, risk assessment, and reporting processes. Built on the Salesforce Platform and AWS, the system emphasizes security and reliability. The company was founded in 2018 by industry veterans with extensive experience in the medical device sector. They claim 30% of MDRs sent to the FDA go through their platform and aim to make post-market surveillance 40% faster for their clients.

Smarteeva is a provider of advanced post-market surveillance solutions for medical device companies, leveraging artificial intelligence (AI) and machine learning to streamline operations and enhance regulatory compliance. Their product suite includes Complaints Management, Recall Management, Adverse Events tracking, and MDREngine, which aggregates medical device regulatory data. Smarteeva's solutions aim to improve customer service, operational efficiency, and patient safety by automating complaint handling, risk assessment, and reporting processes. Built on the Salesforce Platform and AWS, the system emphasizes security and reliability. The company was founded in 2018 by industry veterans with extensive experience in the medical device sector. They claim 30% of MDRs sent to the FDA go through their platform and aim to make post-market surveillance 40% faster for their clients.
What they do: AI-driven post-market surveillance and complaints/adverse-event management software for medical device companies
Founded: 2018
Headcount: 30 employees
Tech base: Built on Salesforce Platform and AWS
Funding (recorded): Seed round (Feb 2019); total funding listed as $500,000 USD
Post-market surveillance and regulatory compliance for medical devices
2018
Healthcare / Medical device software
$500,000.00
Recorded seed round dated Feb 1, 2019; publicly available profiles obfuscate investor names.