What's happening in post-market surveillance and what to do about it.

Regulatory updates, AI in MedTech, complaint management trends, and product news

Blog
June 2, 2026
How Smarteeva Automates IMDRF Code Assignment in Medical Device Complaint Workflows
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Guide
June 9, 2026
The Complete Guide to MDR Reporting for Medical Devices: From Awareness to Submission
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How To
June 4, 2026
How Smarteeva Automates Medical Device Complaint Intake From Email, Forms, and Bulk Files
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How To
June 8, 2026
How Smarteeva Submits an MDR to the FDA in 3 Minutes via ESG NextGen API
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Blog
June 1, 2026
How Smarteeva Cuts Medical Device Complaint Closure Time by 70%
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Guide
June 5, 2026
AI in Post-Market Surveillance: What Actually Works and What Is Still Marketing
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How To
June 4, 2026
How Smarteeva Generates a PSUR in 8 Minutes From Connected Post-Market Data
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Guide
June 3, 2026
The Definitive Guide to Medical Device Complaint Management: Every Stage From Intake to Closure
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Blog
June 1, 2026
eQMS vs Post-Market Surveillance Platform: What MedTech Teams Get Wrong About This Decision
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Blog
May 28, 2026
Manual PMS Reporting vs Automated: What 100+ Hours of Assembly Work Actually Costs
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Blog
March 9, 2026
Infusion Pumps & the Global Crisis: A Smarteeva Perspective
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Blog
March 13, 2026
How Smarteeva’s MAUDE Analysis Reveals the Top MDR Submitters in 2022
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Blog
April 6, 2026
How Smarteeva Maps the Top 5 Post-Market Surveillance Trends for 2024
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Blog
April 9, 2026
How Smarteeva’s UI/UX Design Reduces Training Costs and Complaint Handling Time
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Blog
April 6, 2026
How Smarteeva Reads the MIT Report on 95% AI Project Failure - And Why MedTech Is Different
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Blog
April 3, 2026
How Smarteeva’s Analysis of FDA Data Shows Patient Death Codes Declining as a Percentage of MDRs
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Blog
April 7, 2026
How Smarteeva Identified the Top 5 Trends Reshaping Post-Market Surveillance
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Blog
April 8, 2026
How Smarteeva Enables Proactive Post-Market Surveillance with Real-World Data
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Blog
April 12, 2026
How Smarteeva Automates PMCF Reporting Under EU MDR
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Blog
April 2, 2026
How Smarteeva Closes the Recall Management Gap Between Manufacturers and Healthcare Providers
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Blog
December 2, 2025
From 2.6 Million MDRs to Actionable Insight: How AI Is Changing Post-Market Surveillance
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News
December 1, 2025
Smarteeva ESG NextGen Integration - Direct MDR Submission to FDA Through the New API
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News
December 3, 2025
How SmarteevaAI Deploys Fine-Tuned AI Agents That Automate Complaint Processing Without Developer Support
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Blog
December 3, 2025
AI Effects on Employment: What the Yale Study Misses About How Work Is Actually Changing
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News
December 1, 2025
Smarteeva Orchestra: No-Code AI Agent Builder for MedTech Quality & Regulatory Teams
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Blog
May 1, 2026
How Smarteeva’s Agentic AI Works Inside MedTech Quality Operations
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