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Therapeutic Innovation & Regulatory Science
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May 17, 2023
The Challenges for Manufacturers of the Increased Clinical Evaluation in the European Medical Device Regulations: A Quantitative Study
Breda Kearney, Olivia McDermott
Therapeutic Innovation & Regulatory Science
|
June 17, 2025
The Challenges in the Regulatory Approval of Additive-Manufactured Medical Devices: A Quantitative Survey
Kieran Connole, Olivia McDermott
Heliyon
|
April 15, 2024
Industrial clusters, creating a strategy for continued success
David McKernan, Olivia McDermott
Expert Review of Medical Devices
|
December 2, 2023
The value of using real-world evidence as a source of clinical evidence in the European medical device regulations: a mixed methods study
Olivia McDermott, Breda Kearney
Expert Review of Medical Devices
|
February 17, 2025
The use of predetermined change control plans to enable the release of new versions of software as a medical device
Jacques Andre DuPreez, Olivia McDermott
Hospital Topics
|
March 24, 2022
The Impact of Healthcare 4.0 on the Healthcare Service Quality: A Systematic Literature Review
Michael Sony, Jiju Antony, Olivia McDermott
Reproductive Health
|
March 6, 2022
A comparison of assisted human reproduction (AHR) regulation in Ireland with other developed countries
Olivia McDermott, Lauraine Ronan, Mary Butler
International Journal of Health Care Quality Assurance
|
November 14, 2023
A cross-organizational Lean deployment in an Italian regional healthcare system
Angelo Rosa, Giuliano Marolla, Olivia McDermott
Expert Review of Medical Devices
|
April 13, 2026
The impact of integrating artificial intelligence into regulatory affairs functions in the Medtech industry
Renee Cotta, Mary Garvey, Olivia McDermott
Expert Review of Medical Devices
|
July 10, 2026
Restriction of PFAS use in medical devices - what next for medical device manufacturers?
Martha Folan, Matthew Fitzpatrick, Olivia McDermott
Page
of 2
Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
Therapeutic Innovation & Regulatory Science
|
May 17, 2023
The Challenges for Manufacturers of the Increased Clinical Evaluation in the European Medical Device Regulations: A Quantitative Study
Breda Kearney, Olivia McDermott
Therapeutic Innovation & Regulatory Science
|
June 17, 2025
The Challenges in the Regulatory Approval of Additive-Manufactured Medical Devices: A Quantitative Survey
Kieran Connole, Olivia McDermott
Heliyon
|
April 15, 2024
Industrial clusters, creating a strategy for continued success
David McKernan, Olivia McDermott
Expert Review of Medical Devices
|
December 2, 2023
The value of using real-world evidence as a source of clinical evidence in the European medical device regulations: a mixed methods study
Olivia McDermott, Breda Kearney
Expert Review of Medical Devices
|
February 17, 2025
The use of predetermined change control plans to enable the release of new versions of software as a medical device
Jacques Andre DuPreez, Olivia McDermott
Hospital Topics
|
March 24, 2022
The Impact of Healthcare 4.0 on the Healthcare Service Quality: A Systematic Literature Review
Michael Sony, Jiju Antony, Olivia McDermott
Reproductive Health
|
March 6, 2022
A comparison of assisted human reproduction (AHR) regulation in Ireland with other developed countries
Olivia McDermott, Lauraine Ronan, Mary Butler
International Journal of Health Care Quality Assurance
|
November 14, 2023
A cross-organizational Lean deployment in an Italian regional healthcare system
Angelo Rosa, Giuliano Marolla, Olivia McDermott
Expert Review of Medical Devices
|
April 13, 2026
The impact of integrating artificial intelligence into regulatory affairs functions in the Medtech industry
Renee Cotta, Mary Garvey, Olivia McDermott
Expert Review of Medical Devices
|
July 10, 2026
Restriction of PFAS use in medical devices - what next for medical device manufacturers?
Martha Folan, Matthew Fitzpatrick, Olivia McDermott
Page
of 2