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MedTech Strategist, Market Pathways, and the Community Blog are pleased to feature thought leadership contributed by medical device industry executives, regulators, consultants, investors, clinical KOLs, and other experts from the global medtech community.

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Regulatory & Reimbursement

From Complaint Handling to Active Surveillance: Why 2026 Marks a Turning Point for Device Safety Monitoring

  • 2026-04-24 00:00:00.0
  • Contributing Writer
  • Market Pathways

Regulators in the EU, UK, and US already mandate the structured capture of medical device safety data. Now they are beginning to analyze it, and they expect device manufacturers to be doing the same. Existing capabilities, however, may hold companies back, warns Qinecsa’s Jonathan Messer.

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