Tag: Postmarketing surveillance

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Recent Related Articles to Postmarketing surveillance

4 Day Virtual Medical Device Software Compliance Course: Complying with the EU MDR ...

Added to Collection on: 2024-03-29 19:47:47

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Regulation of medical devices
Medical device
Regulation (EU) 2017/745
IEC 62304
Regulation (EU) 2017/746
Notified body
Design controls
Validation
Postmarketing surveillance
Technical file
Software of unknown pedigree
Agile software development

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UK Government Propose International Medical Device Recognition Framework

Added to Collection on: 2024-05-21 18:54:15

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Regulation of medical devices
Medical device
Medicines and Healthcare products Regulatory Agency
UKCA marking
Postmarketing surveillance
United Kingdom

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FDA to launch 'active' monitory system to improve medical device safety

Added to Collection on: 2024-09-18 22:08:12

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Food and Drug Administration
Medical device
Diana Zuckerman
FDA Center for Devices and Radiological Health
National Center for Health Research
Federal Food, Drug, and Cosmetic Act
Single Use Medical Device Reprocessing
Postmarketing surveillance

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MHRA Updates its Timeline for Medical Device Regulatory Changes in the UK | JD Supra

Added to Collection on: 2024-10-14 20:20:58

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

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JPM2025: Regulation of artificial intelligence: Navigating a new frontier in health care

Added to Collection on: 2025-01-07 17:49:43

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Regulation of artificial intelligence
Regulation of medical devices
Clinical research
Computational neuroscience
Health informatics
Medical device
Artificial intelligence
Regulation (EU) 2017/745
Postmarketing surveillance
Medicines and Healthcare products Regulatory Agency
Applications of artificial intelligence
Real world data
United Kingdom

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What is next for medical devices? New post-market surveillance obligations and beyond…

Added to Collection on: 2025-06-17 15:59:58

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Regulation of medical devices
Regulation (EU) 2017/745
Postmarketing surveillance
Medical device
Regulation (EU) 2017/746
Unique Device Identification
UKCA marking
Medicines and Healthcare products Regulatory Agency
FDA Center for Devices and Radiological Health

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AI Testing and Evaluation: Learnings from pharmaceuticals and medical devices - Microsoft

Added to Collection on: 2025-07-07 16:03:23

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Clinical research
Regulation of medical devices
Pharmaceuticals policy
Clinical trials
Health care
Medical device
Food and Drug Administration
Regulation (EU) 2017/745
Postmarketing surveillance
Digital health
Internet of things
United States

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MHRA announces proposals to improve access to world's best medical devices for patients ...

Added to Collection on: 2025-07-21 23:05:53

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Regulation of medical devices
Medicines and Healthcare products Regulatory Agency
Medical device
Postmarketing surveillance
ISO 13485
Regulation (EU) 2017/745
Food and Drug Administration
Regulation (EU) 2017/746
MHRA
Global Medical Device Nomenclature
United Kingdom

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Health institutions to have say in MHRA's reforms for in-house manufactured medtech

Added to Collection on: 2025-08-15 16:05:18

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Regulation of medical devices
Canary Wharf
Department of Health and Social Care
Medicines and Healthcare products Regulatory Agency
Clinical trials
Postmarketing surveillance
Medical device
National Health Service
MHRA
Shutterstock.com
United Kingdom

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European Union calls for evidence on simplifying medical device rules - JD Supra

Added to Collection on: 2025-09-17 20:24:51

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Regulation of medical devices
Regulation (EU) 2017/746
Regulation (EU) 2017/745
Medical device
MDR
Artificial Intelligence Act
CE marking
Regulation (EU) No. 305/2011
European authorised representative
Postmarketing surveillance

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