Tag: Regulation (EU) 2017/745

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Recent Related Articles to Regulation (EU) 2017/745

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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ANDHealth & TGA extend partnership - BioMelbourne Network

Added to Collection on: 2024-08-18 23:57:50

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Health informatics
Regulation of medical devices
SAMD
Digital health
Medical software
Medical device
Health technology
Regulation (EU) 2017/745
Digital therapeutics

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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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A Look Ahead in Life Sciences: What We Are Tracking in the Fourth Quarter of 2024 and Beyond

Added to Collection on: 2024-10-01 19:19:16

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Regulation of medical devices
Food and Drug Administration
Clinical research
Pharmaceuticals policy
Clinical trials
Postmarketing surveillance
Medical device
Medicines and Healthcare products Regulatory Agency
Biosimilar
Regulation (EU) 2017/745
Investigational device exemption
FDA Center for Devices and Radiological Health

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Medical Devices Outsourcing Market Size to Reach USD 232.8 Billion by 2028, Growing at ...

Added to Collection on: 2024-10-03 14:22:31

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Economic globalization
Offshoring
Medical devices
Business management
International business
Outsourcing
Medical device
Regulation (EU) 2017/745
Business process outsourcing in the Philippines
United States
Wilmington

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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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Medical Device Outsourcing Market To Surge US$ 352.3 Billion By 2032

Added to Collection on: 2025-01-03 18:20:58

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Regulation of medical devices
Economic globalization
Offshoring
Information technology management
Food and Drug Administration
Medical device
Outsourcing
Regulatory affairs
Contract manufacturing organization
Regulation (EU) 2017/745
Federal Food, Drug, and Cosmetic Act
Single Use Medical Device Reprocessing

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Medical-device industry divided on Health Ministry clarification ending import of refurbished items

Added to Collection on: 2025-01-17 23:07:29

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Health care
Medical device
Central Drugs Standard Control Organisation
Make in India
Regulation (EU) 2017/745
Health technology
India

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