Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Tom Melvin

Showing results (11-20 of 25) with videos related to

Pageof 3
Sort By:
Expert Review of Medical Devices|January 8, 2026
Regulatory readiness for innovation: a mixed-methods study of national competent authority professional and organizational capacities in the context of pre-market clinical investigations and early feasibility studiesMajella Geraghty, Francesco Malandrini, Giuditta Callea, et al.
Scientific Reports|September 9, 2024
The regulatory status of health apps that employ gamificationOscar Freyer, Kamil J Wrona, Quentin de Snoeck, et al.
Journal of Medical Internet Research|October 1, 2025
Stakeholder Perspectives on Early Feasibility Studies for Digital Health Technologies in the European Union: Qualitative Interview StudyMarlen Peseke, Ilja Michaelis, Ornella Tangila Kayembe, et al.
EFORT Open Reviews|November 1, 2023
Clinical investigations to evaluate high-risk orthopaedic devices: a systematic review of the peer-reviewed medical literatureAnne Lübbeke, Christophe Combescure, Christophe Barea, et al.
Annals of Cardiothoracic Surgery|October 22, 2024
How to advance from minimally invasive coronary artery bypass grafting to totally endoscopic coronary bypass grafting: challenges in Europe versus United States of AmericaMichiel Algoet, Tom Melvin, Stepan Cerny, et al.
Clinical Chemistry and Laboratory Medicine|August 19, 2025
Urgent call to the European Commission to simplify and contextualize IVDR Article 5.5 for tailored and precision diagnosticsChrista Cobbaert, Christian Schweiger, Christoph Buchta, et al.
Trials|January 20, 2025
Large simple randomized controlled trials-from drugs to medical devices: lessons from recent experienceSergio Buccheri, Stefan James, Marion Mafham, et al.
Acta Orthopaedica|November 25, 2024
Safety notices and registry outlier data measure different aspects of safety and performance of total knee implants: a comparative study of safety notices and register outliersLotje A Hoogervorst, Yijun Ren, Tom Melvin, et al.
Clinical Therapeutics|July 3, 2026
Early Feasibility Studies in Europe: A Multisite Qualitative Study of Operational Challenges and Site Selection Determinants at 6 University HospitalsAdrian Valledor, Ornella Tangila Kayembe, Daniel Beltran, et al.
European Heart Journal|August 28, 2023
Quality and transparency of evidence for implantable cardiovascular medical devices assessed by the CORE-MD consortiumGeorge C M Siontis, Bernadette Coles, Jonas D Häner, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Expert Review of Medical Devices|January 8, 2026
Regulatory readiness for innovation: a mixed-methods study of national competent authority professional and organizational capacities in the context of pre-market clinical investigations and early feasibility studiesMajella Geraghty, Francesco Malandrini, Giuditta Callea, et al.
Scientific Reports|September 9, 2024
The regulatory status of health apps that employ gamificationOscar Freyer, Kamil J Wrona, Quentin de Snoeck, et al.
Journal of Medical Internet Research|October 1, 2025
Stakeholder Perspectives on Early Feasibility Studies for Digital Health Technologies in the European Union: Qualitative Interview StudyMarlen Peseke, Ilja Michaelis, Ornella Tangila Kayembe, et al.
EFORT Open Reviews|November 1, 2023
Clinical investigations to evaluate high-risk orthopaedic devices: a systematic review of the peer-reviewed medical literatureAnne Lübbeke, Christophe Combescure, Christophe Barea, et al.
Annals of Cardiothoracic Surgery|October 22, 2024
How to advance from minimally invasive coronary artery bypass grafting to totally endoscopic coronary bypass grafting: challenges in Europe versus United States of AmericaMichiel Algoet, Tom Melvin, Stepan Cerny, et al.
Clinical Chemistry and Laboratory Medicine|August 19, 2025
Urgent call to the European Commission to simplify and contextualize IVDR Article 5.5 for tailored and precision diagnosticsChrista Cobbaert, Christian Schweiger, Christoph Buchta, et al.
Trials|January 20, 2025
Large simple randomized controlled trials-from drugs to medical devices: lessons from recent experienceSergio Buccheri, Stefan James, Marion Mafham, et al.
Acta Orthopaedica|November 25, 2024
Safety notices and registry outlier data measure different aspects of safety and performance of total knee implants: a comparative study of safety notices and register outliersLotje A Hoogervorst, Yijun Ren, Tom Melvin, et al.
Clinical Therapeutics|July 3, 2026
Early Feasibility Studies in Europe: A Multisite Qualitative Study of Operational Challenges and Site Selection Determinants at 6 University HospitalsAdrian Valledor, Ornella Tangila Kayembe, Daniel Beltran, et al.
European Heart Journal|August 28, 2023
Quality and transparency of evidence for implantable cardiovascular medical devices assessed by the CORE-MD consortiumGeorge C M Siontis, Bernadette Coles, Jonas D Häner, et al.
Pageof 3