Smarteeva

Booth #902. Charlotte. 15 to 17 September. We're exhibiting at #RAPS Convergence 2026. Come and tell us where post-market surveillance is costing you time, and we'll show you what it looks like when complaints, adverse events, MDR filings, recalls, and risk sit in one Salesforce-native platform. Jaime Castillo Ayub Castillo is at the booth all 3 days. Book a slot: https://lnkd.in/dfRAdtpe #RAPSConvergence #RegulatoryAffairs #MedicalDevices

If your goal is measurable change, don’t buy an experiment. The MIT report essentially points to a divide: organizations succeed more often when they partner with specialized product companies instead of trying to custom-build everything internally. In regulated environments, this matters even more because adoption must be practical and validation-ready. The AI that wins is the AI that ships inside the process, learns from feedback, and improves outcomes.

The Yale study says AI hasn’t disrupted the labor market visibly. That may be true at the national level. But inside companies, AI is already changing the day-to-day reality: the same teams are being asked to cover more volume, faster, with fewer gaps. If you’re in Quality, Regulatory, or Post-Market, you’ve felt the shift: higher throughput targets, faster response expectations, and less tolerance for rework. See how we apply this in complaints & MDR 🔽

One product. Many markets. Different rules. Smarteeva helps Regulatory teams manage global submissions and approvals in one place - covering FDA, EU MDR, and beyond.

From 1 hour to 6 minutes per complaint. Smarteeva streamlines case creation, verification, classification, and duplicate detection, so your team stays consistent and inspection-ready.

Smarteeva's AI-driven classification engine optimizes complaint triage by eliminating review redundancy and human error factors, accelerating complaint resolution and FDA submissions. Read how: https://lnkd.in/gWAMmXt9 #InsightswithSmarteeva #Medtech #complaintmanagement #Pharma #Smarteeva #biotech #medtechtrends #medtechindustry #medicaltechnology #technology #health #medicaldevicediagnostics #ai #mdr #recalls #complaints #mir #fda #cvr