Tag: Regulation (EU) 2017/746

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Recent Related Articles to Regulation (EU) 2017/746

Domino solutions protect patients from counterfeit medical devices - Cambridge Network

Added to Collection on: 2024-05-24 17:56:44

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Regulation of medical devices
Medical devices
Health care
Food and Drug Administration
Medical device
Cybernetics
Regulation (EU) 2017/745
Unique Device Identification
Regulation (EU) 2017/746
Artificial cardiac pacemaker

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Element introduces regulatory intelligence platform for medical devices

Added to Collection on: 2024-06-18 21:54:45

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Regulation of medical devices
Medical devices
Health care
Medical device
Food and Drug Administration
Regulation (EU) 2017/745
Regulation (EU) 2017/746

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In Vitro Diagnostics (IVD) Market Predicted to Hit $149.4 Billion

Added to Collection on: 2024-08-09 13:13:35

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Medical tests
Biotechnology
Molecular diagnostics
IVD
Regulation (EU) 2017/746
Point-of-care testing
Qiagen
Thermo Fisher Scientific
Personalized medicine
Laboratory developed test
Abionic

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In Vitro Diagnostic Quality Control Strategy & Trends Report 2024 - Yahoo Finance

Added to Collection on: 2024-08-26 13:38:54

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Medical tests
Regulation of medical devices
Biotechnology
Molecular diagnostics
Regulation (EU) 2017/746
Point-of-care testing
Seegene
IVD
Regulation (EU) 2017/745
Thermo Fisher Scientific
DiaSorin

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Balancing innovation and safety: The impact of Medtech regulations - Pharmaphorum

Added to Collection on: 2024-09-09 13:45:37

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Regulation of artificial intelligence
Existential risk from artificial general intelligence
Cybernetics
Computer law
Computational neuroscience
Artificial intelligence
Artificial Intelligence Act
Regulatory compliance
Regulation (EU) 2017/746
Occupational safety and health
Artificial intelligence in healthcare

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Irish Medtech call for EU regulatory reform as leaders gather in Galway

Added to Collection on: 2024-10-24 00:30:34

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Medtech
Zimmer Biomet Robotics
Harmonization
Regulation (EU) 2017/746

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Medtech Conference recap: New CDRH leader details approach; AI and LDTs in focus

Added to Collection on: 2024-10-23 20:06:20

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Health care
Medical device
Johnson & Johnson
Abbott Laboratories
Medtech
Regulation (EU) 2017/746

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European Parliament calls for proposals to reform MDR and IVDR by end of Q1

Added to Collection on: 2024-10-24 15:19:09

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Regulation of medical devices
Regulation (EU) 2017/746
Regulation (EU) 2017/745
Věra Jourová
Liese
Medical device
Medtech
Stella Kyriakides
Parliament of Singapore
MedTech Europe
European Parliament

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Understanding the changes and impact of MDR and IVDR - Medical Design & Outsourcing

Added to Collection on: 2024-11-05 22:13:58

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Regulation of medical devices
Regulation (EU) 2017/745
Regulation (EU) 2017/746
Medical device
Unique Device Identification
Regulatory affairs
Quality management system
IVDR
Regulatory compliance
CE marking
Postmarketing surveillance

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How to prepare for the MDR and IVDR transition - Medical Design & Outsourcing

Added to Collection on: 2024-11-06 04:14:01

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Regulation of medical devices
Regulation (EU) 2017/746
Regulation (EU) 2017/745
Medical device
Regulatory affairs
Quality management system
Quality assurance
Quality management
Regulatory agency
Restriction of Hazardous Substances Directive
Compliance

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