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IEEE Journal of Translational Engineering in Health and Medicine
|
August 25, 2022
The European Medical Device Regulation-What Biomedical Engineers Need to Know
Tom Melvin
EFORT Open Reviews
|
July 18, 2019
New medical device regulations: the regulator's view
Tom Melvin, Marina Torre
Diabetic Medicine : a Journal of the British Diabetic Association
|
October 24, 2023
A European regulatory pathway for Tidepool loop following clearance in the United States?
Laura Downey, Shane O'Donnell, Tom Melvin, et al.
NPJ Digital Medicine
|
January 31, 2023
Can Apple and Google continue as health app gatekeepers as well as distributors and developers?
Olamide Sadare, Tom Melvin, Hugh Harvey, et al.
Mayo Clinic Proceedings. Digital Health
|
April 10, 2025
Continuous Improvement of Digital Health Applications Linked to Real-World Performance Monitoring: Safe Moving Targets?
Stephen Gilbert, Andreia Pimenta, Ashley Stratton-Powell, et al.
Frontiers in Medicine
|
June 30, 2026
Regulatory Science: exploring an emerging scientific discipline in health care
Laura Volpi, Michael D'Agosto, Tom Melvin, et al.
Journal of Medical Internet Research
|
April 14, 2023
Learning From Experience and Finding the Right Balance in the Governance of Artificial Intelligence and Digital Health Technologies
Stephen Gilbert, Stuart Anderson, Martin Daumer, et al.
Pediatric Research
|
September 27, 2023
Evidence from clinical trials on high-risk medical devices in children: a scoping review
Kathrin Guerlich, Bernadeta Patro-Golab, Paulina Dworakowski, et al.
EFORT Open Reviews
|
November 11, 2021
Improved clinical investigation and evaluation of high-risk medical devices: the rationale and objectives of CORE-MD (Coordinating Research and Evidence for Medical Devices)
Alan G Fraser, Rob G H H Nelissen, Per Kjærsgaard-Andersen, et al.
Expert Review of Medical Devices
|
September 20, 2024
Orphan and paediatric medical devices in Europe: recommendations to support their availability for on-label and off-label clinical indications
Tom Melvin, Marc M Dooms, Berthold Koletzko, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 25) with videos related to
Sort By:
Page
of 3
IEEE Journal of Translational Engineering in Health and Medicine
|
August 25, 2022
The European Medical Device Regulation-What Biomedical Engineers Need to Know
Tom Melvin
EFORT Open Reviews
|
July 18, 2019
New medical device regulations: the regulator's view
Tom Melvin, Marina Torre
Diabetic Medicine : a Journal of the British Diabetic Association
|
October 24, 2023
A European regulatory pathway for Tidepool loop following clearance in the United States?
Laura Downey, Shane O'Donnell, Tom Melvin, et al.
NPJ Digital Medicine
|
January 31, 2023
Can Apple and Google continue as health app gatekeepers as well as distributors and developers?
Olamide Sadare, Tom Melvin, Hugh Harvey, et al.
Mayo Clinic Proceedings. Digital Health
|
April 10, 2025
Continuous Improvement of Digital Health Applications Linked to Real-World Performance Monitoring: Safe Moving Targets?
Stephen Gilbert, Andreia Pimenta, Ashley Stratton-Powell, et al.
Frontiers in Medicine
|
June 30, 2026
Regulatory Science: exploring an emerging scientific discipline in health care
Laura Volpi, Michael D'Agosto, Tom Melvin, et al.
Journal of Medical Internet Research
|
April 14, 2023
Learning From Experience and Finding the Right Balance in the Governance of Artificial Intelligence and Digital Health Technologies
Stephen Gilbert, Stuart Anderson, Martin Daumer, et al.
Pediatric Research
|
September 27, 2023
Evidence from clinical trials on high-risk medical devices in children: a scoping review
Kathrin Guerlich, Bernadeta Patro-Golab, Paulina Dworakowski, et al.
EFORT Open Reviews
|
November 11, 2021
Improved clinical investigation and evaluation of high-risk medical devices: the rationale and objectives of CORE-MD (Coordinating Research and Evidence for Medical Devices)
Alan G Fraser, Rob G H H Nelissen, Per Kjærsgaard-Andersen, et al.
Expert Review of Medical Devices
|
September 20, 2024
Orphan and paediatric medical devices in Europe: recommendations to support their availability for on-label and off-label clinical indications
Tom Melvin, Marc M Dooms, Berthold Koletzko, et al.
Page
of 3