# 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**  
[Read article](/content/blog/how-smarteeva-automates-imdrf-code-assignment/index.html)

**Guide**  
**June 9, 2026**  
**The Complete Guide to MDR Reporting for Medical Devices: From Awareness to Submission**  
[Read article](/content/blog/complete-guide-mdr-reporting-medical-devices/index.html)

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**How To**  
**June 4, 2026**  
**How Smarteeva Automates Medical Device Complaint Intake From Email, Forms, and Bulk Files**  
[Read article](/content/blog/how-smarteeva-automates-medical-device-complaint-intake/index.html)

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**How To**  
**June 8, 2026**  
**How Smarteeva Submits an MDR to the FDA in 3 Minutes via ESG NextGen API**  
[Read article](/content/blog/how-smarteeva-submits-mdr-to-fda-in-3-minutes/index.html)

**Blog**  
**June 1, 2026**  
**How Smarteeva Cuts Medical Device Complaint Closure Time by 70%**  
[Read article](/content/blog/how-smarteeva-cuts-complaint-closure-time-by-70-percent/index.html)

**Guide**  
**June 5, 2026**  
**AI in Post-Market Surveillance: What Actually Works and What Is Still Marketing**  
[Read article](/content/blog/ai-in-post-market-surveillance-what-actually-works/index.html)

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**How To**  
**June 4, 2026**  
**How Smarteeva Generates a PSUR in 8 Minutes From Connected Post-Market Data**  
[Read article](/content/blog/how-smarteeva-generates-psur-in-8-minutes/index.html)

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**Guide**  
**June 3, 2026**  
**The Definitive Guide to Medical Device Complaint Management: Every Stage From Intake to Closure**  
[Read article](/content/blog/definitive-guide-medical-device-complaint-management/index.html)

**Blog**  
**June 1, 2026**  
**eQMS vs Post-Market Surveillance Platform: What MedTech Teams Get Wrong About This Decision**  
[Read article](/content/blog/eqms-vs-post-market-surveillance-platform/index.html)

**Blog**  
**May 28, 2026**  
**Manual PMS Reporting vs Automated: What 100+ Hours of Assembly Work Actually Costs**  
[Read article](/content/blog/manual-vs-automated-pms-reporting/index.html)

**Blog**  
**March 9, 2026**  
**Infusion Pumps & the Global Crisis: A Smarteeva Perspective**  
[Read article](/content/blog/infusion-pump-recall-crisis-baxter-bd-smiths-medical/index.html)

**Blog**  
**March 13, 2026**  
**How Smarteeva’s MAUDE Analysis Reveals the Top MDR Submitters in 2022**  
[Read article](/content/blog/top-mdr-submitters-2022-smarteeva-maude-analysis/index.html)

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**Blog**  
**April 6, 2026**  
**How Smarteeva Maps the Top 5 Post-Market Surveillance Trends for 2024**  
[Read article](/content/blog/top-5-post-market-surveillance-trends-2024/index.html)

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**Blog**  
**April 9, 2026**  
**How Smarteeva’s UI/UX Design Reduces Training Costs and Complaint Handling Time**  
[Read article](/content/blog/how-smarteeva-ui-ux-reduces-training-costs-complaint-handling/index.html)

**Blog**  
**April 6, 2026**  
**How Smarteeva Reads the MIT Report on 95% AI Project Failure - And Why MedTech Is Different**  
[Read article](/content/blog/mit-report-95-ai-failure-medtech-different/index.html)

**Blog**  
**April 3, 2026**  
**How Smarteeva’s Analysis of FDA Data Shows Patient Death Codes Declining as a Percentage of MDRs**  
[Read article](/content/blog/patient-death-codes-declining-percentage-mdrs/index.html)

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**Blog**  
**April 7, 2026**  
**How Smarteeva Identified the Top 5 Trends Reshaping Post-Market Surveillance**  
[Read article](/content/blog/how-smarteeva-identified-the-top-5-trends-reshaping-post-market-surveillance/index.html)

**Blog**  
**April 8, 2026**  
**How Smarteeva Enables Proactive Post-Market Surveillance with Real-World Data**  
[Read article](/content/blog/how-smarteeva-enables-proactive-post-market-surveillance-with-real-world-data/index.html)

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**Blog**  
**April 12, 2026**  
**How Smarteeva Automates PMCF Reporting Under EU MDR**  
[Read article](/content/blog/how-smarteeva-automates-pmcf-reporting-under-eu-mdr/index.html)

**Blog**  
**April 2, 2026**  
**How Smarteeva Closes the Recall Management Gap Between Manufacturers and Healthcare Providers**  
[Read article](/content/blog/recall-management-gap-between-manufacturers-and-healthcare-providers/index.html)

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**Blog**  
**December 2, 2025**  
**From 2.6 Million MDRs to Actionable Insight: How AI Is Changing Post-Market Surveillance**  
[Read article](/content/blog/how-ai-is-changing-post-market-surveillance-medtech/index.html)

**News**  
**December 1, 2025**  
**Smarteeva ESG NextGen Integration - Direct MDR Submission to FDA Through the New API**  
[Read article](/content/blog/smarteeva-esg-nextgen-api-fda-mdr-submission/index.html)

**News**  
**December 3, 2025**  
**How SmarteevaAI Deploys Fine-Tuned AI Agents That Automate Complaint Processing Without Developer Support**  
[Read article](/content/blog/smarteevaai-five-ai-agents-post-market-surveillance-complaint-processing/index.html)

**Blog**  
**December 3, 2025**  
**AI Effects on Employment: What the Yale Study Misses About How Work Is Actually Changing**  
[Read article](/content/blog/ai-effects-on-employment-yale-study-review/index.html)

**News**  
**December 1, 2025**  
**Smarteeva Orchestra: No-Code AI Agent Builder for MedTech Quality & Regulatory Teams**  
[Read article](/content/blog/smarteeva-orchestra-ai-agent-builder-quality-regulatory-teams/index.html)

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**Blog**  
**May 1, 2026**  
**How Smarteeva’s Agentic AI Works Inside MedTech Quality Operations**  
[Read article](/content/blog/how-smarteeva-agentic-ai-works-medtech-quality-operations/index.html)