Tag: Regulation (EU) 2017/745

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Celegence adds new feature for efficient compliance documentation - Med-Tech Innovation

Added to Collection on: 2022-07-08 13:34:47

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Articles
Health
Technology
Regulation (EU) 2017/746
Regulation (EU) 2017/745
Clinical research
Clinical trials
Pharmaceuticals policy
Medical device
Medical devices
Notified body
Postmarketing surveillance
CAPTIS
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IoT cyber security impetus placed on manufacturers - TÜV SÜD - Smart Energy International

Added to Collection on: 2022-07-23 16:50:22

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Technology
Articles
Cyberwarfare
Computing
Computer security
Ambient intelligence
Digital technology
Internet of things
IT security standards
Regulation (EU) 2017/745
Technischer Überwachungsverein
Security convergence

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Column - EU MDR: Ensuring Labeling Compliance - MedTech Intelligence

Added to Collection on: 2023-10-25 23:51:28

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Regulation of medical devices
Regulation (EU) 2017/745
Regulation (EU) 2017/746
Unique Device Identification
Medical device
MDR
CE marking
Packaging and labeling
Design controls
Single Use Medical Device Reprocessing

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Wandong Medical's full-line products obtain the MDR certification, facilitating its entry to the ...

Added to Collection on: 2023-12-15 14:55:18

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Regulation of medical devices
Regulation (EU) 2017/745
Medical device
Magnetic resonance imaging
Medical imaging
MDR
Regulation (EU) 2017/746
mri systems

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How is Europe's MedTech industry navigating the EU MDR? - Medical Device Network

Added to Collection on: 2024-01-11 15:20:04

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Clinical research
Regulation of medical devices
Pharmaceuticals policy
Artificial intelligence
Cybernetics
Medical device
Regulation (EU) 2017/745
Clinical trial
Regulation (EU) 2017/746
Contract research organization

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European Commission proposes delays for IVDR to prevent supply disruption

Added to Collection on: 2024-01-24 18:27:24

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Regulation of medical devices
Regulation (EU) 2017/746
Regulation (EU) 2017/745
Medical device
Notified body
MedTech Europe
Medtech

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European Commission Proposes Extension for EU IVDR Compliance

Added to Collection on: 2024-01-24 18:21:41

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Regulation of medical devices
Regulation (EU) 2017/745
Regulation (EU) 2017/746
Medical device
Medicines and Healthcare products Regulatory Agency
Postmarketing surveillance

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FDA To Host Town Hall on Medical Device Sterilization - MedTech Intelligence

Added to Collection on: 2024-01-25 00:21:41

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Biocides
Food and Drug Administration
Regulation of medical devices
IARC Group 1 carcinogens
Health care
Medical device
Sterilization
FDA Center for Devices and Radiological Health
Ethylene oxide
ETO
Regulation (EU) 2017/745
Anprolene

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X-Nav Technologies' X-Guide® System First to Receive EU Medical Device Regulation Certification

Added to Collection on: 2024-03-12 14:17:11

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Regulation of medical devices
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Regulation (EU) 2017/745
Computer-assisted surgery
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Quality management system
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X-Nav Technologies LLC

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Asuragen's QuantideX diagnostic test secures IVDR certification - Medical Device Network

Added to Collection on: 2024-03-25 18:27:16

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Regulation of medical devices
Medical tests
Regulation (EU) 2017/746
Philadelphia chromosome
Chronic myelogenous leukemia
Molecular diagnostics
ABL
Regulation (EU) 2017/745
Bio-Techne
Biomarker
Real-time polymerase chain reaction

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