Why is "Regulation (EU) 2017/745" trending?
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- Ranking position: #
- Date: 2026-04-03 17:09:21
This topic has appeared in the trending rankings 1 time(s) in the past year. While it does not trend frequently, its appearance suggests a renewed or concentrated surge of public interest.
Based on Wikipedia pageviews and search interest, this topic gained significant attention on the selected date.
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Wikipedia Overview
Regulation (EU) 2017/745 is a regulation of the European Union on the clinical investigation and placing on the market of medical devices for human use. It repealed Directive 93/42/EEC on Medical Devices (MDD) and Directive 90/385/EEC on active implantable medical devices (AIMDD).
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Trending Topic Today
Search Interest Perspective
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3D Systems granted full-scope certification under EU Medical Device Regulation 2017/745 - tctmagazine.com
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European Commission’s proposal to amend the MDR and IVDR - www.hoganlovells.com
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InGeneron, Inc. Announces EU Quality Management System Certificate Under MDR Regulation (EU) 2017/745 for Medical Devices - Business Wire
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EU MDR: When Products Without An Intended Medical Purpose Meet Medicinal Substances - Med Device Online
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European Commission launches consultation to streamline MedTech regulation - Med-Tech Insights
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Bot Image, Inc. Earns CE Mark Certification for ProstatID® AI Prostate MRI Software Under EU MDR - PR Newswire
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Clarity on distributors' responsibilities regarding medical devices - Bech-Bruun
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EU Medical Device Regulation - Jones Day
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The EU Data Act Has Arrived - JD Supra
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Medical Device Regulation comes into application - European Medicines Agency (EMA)
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Impulse Dynamics' Quality Management System Receives Certification Under European Union Medical Device Regulation - dicardiology.com
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Regulation 2017/745 on medical devices, two major innovations: 1) the physiological action of devices consisting of natural materials such as vegetal matrices; 2) the chemical-physical-mechanical action of devices made of “substances”, which as such are arti - Frontiers
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Combination Products Under EU MDR 2017/745 - BioProcess International
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Zoll AED 3 Receives EU MDR Certification - respiratory-therapy.com
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The EU’s Medical Device Regulation (EU) 2017/745 – Are You Ready for Huge Sweeping Changes? - In Compliance Magazine
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EU and US Regulatory Challenges Facing AI Health Care Innovator Firms - Stanford Law School
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EC Rep To EU Rep: The Symbol Shift You Can't Ignore - Med Device Online
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Medical devices: new guidance for industry and notified bodies - European Medicines Agency (EMA)
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EU Proposes Extended Deadlines for MDR and IVDR - Jones Day
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EU Commission Updates MDR/IVDR Transitional Provisions - In Compliance Magazine
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Zoll AED Plus Receives EU MDR Certification - respiratory-therapy.com
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EU Regulation Is Driving Medical Device Manufacturers From EU Market - Quality Digest
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Neo Medical’s Spine Care Platform Fully Approved Under EU Medical Device Regulation Directive - BioSpace
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Medical device regulation: landscape and trends - Elsevier
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Paragonix Secures EU MDR Approval for Five Organ Preservation Devices - Business Wire
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Shape Memory Medical wins EU MDR Class III certification for IMPEDE embolization devices - Medical Economics
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European Parliament confirms extension of MDR transition periods - Dentons
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The Role Of The Contract Manufacturer Under The EU MDR & IVDR - Med Device Online
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Call for change to EU medical device regulatory regime: implications for the AI Act - Taylor Wessing
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Portugal implements EU medical device regulation - Garrigues
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Regen Lab Announces the Obtention of the New CE Certification Under Medical Device Regulation (EU MDR 2017/745) Validating the Safety and Performance of Its Proprietary Best-in-class PRP Solutions, Alone or Combined With Hyaluronic Acid - Business Wire
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Medical Devices and IVD’s – The Main Regulatory Changes in 2024 - Med-Tech Insights
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Decision time for UK medical device regulation: diverge or converge with the EU? - Osborne Clarke
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Medical Devices Regulations – obligation to notify supply issues commences on 10 January 2025 - Arthur Cox LLP
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EU advocate general clarifies medical device classification and distributor duties - Osborne Clarke
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MDCG guidance on QMS certification of distributors/importers relabeling, repackaging medical devices - www.hoganlovells.com
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Proposed Amendments to the EU Medical Device Regulation - Taylor Wessing
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TUEV SUED awards one of the first certificates based on Annex XVI of EU Regulation 2017/745 to DEKA - TÜV SÜD
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Frequently Asked Questions on Medical Device Regulation - TÜV SÜD
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France: Publication of the ordinance adapting French law to the EU Regulation on medical devices - Global Compliance News
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Introducing a New Legal Framework, Fees, and Charges - PharmTech.com
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Medical devices and the EU AI Act AI Act - how will two sets of regulations work together? - Taylor Wessing
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Panel for the Future of Science and Technology (STOA) - European Parliament
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Defib manufacturer gains EU regulatory approval - Emergency Services Times
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Medical uses of radiation - energy.ec.europa.eu
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Software under the medical devices regulations - Simmons & Simmons
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Clinical research with a medical device (MDR) - UZ Leuven
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Inspire Medical Systems, Inc. Announces CE Mark Certification under the European Union’s Medical Device Regulation for Inspire Therapy - Finansavisen
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