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October 14, 2026BMJOpen Access

Postmarketing surveillance of medical devices

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Abstract

Spontaneous reporting systems and clinical registries serve complementary purposes

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Cite This Study

Koji Todaka (2026) studied this question.

synapsesocial.com/papers/6ad30f63709cd65f49744109 https://doi.org/10.1136/bmj-2026-101065

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Long-term active surveillance of implantable medical devices: an analysis of factors determining whether current registries are adequate to expose safety and efficacy problemsreview · 2019 · 10 citations
2Detection algorithms and attentive points of safety signal using spontaneous reporting systems as a clinical data sourceClinical Trial · 2021 · 285 citations
3Medical Devices and Real-World Data: Can We Improve Surveillance? Comment on "Quality and Utility of European Cardiovascular and Orthopaedic Registries for the Regulatory Evaluation of Medical Device Safety and Performance Across the Implant Lifecycle: A Systematic Review"Systematic Review · 2026 · 1 citations
4WHO Strategy for Collecting Safety Data in Public Health Programmes: Complementing Spontaneous Reporting SystemsOriginal Research · 2013 · 235 citations
5Postmarket Surveillance of Neuroendovascular Devicesreview · 2024 · 2 citations

More related papers

Advancing Public Health Through Internationally Coordinated Medical Device Registries Comment on "Quality and Utility of European Cardiovascular and Orthopaedic Registries for the Regulatory Evaluation of Medical Device Safety and Performance Across the Implant Lifecycle: A Systematic Review"2026
Post-Marketing Surveillance and Pharmacovigilance: Regulatory Responsibilities and Emerging Challenges2026
Automated Surveillance to Detect Postprocedure Safety Signals of Approved Cardiovascular Devices2010

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