Medical Device Development Process, and Associated Risks and Legislative Aspects-Systematic Review
Objective: Medical device development, from the product's conception to release to market, is very complex and relies significantly on the application of exact processes. This paper aims to provide an analysis and summary of current research in the field of medical device development methodolog...
Main Authors: | Petra Marešová, Blanka Klímová, Jan Honegr, Kamil Kuča, Wan Nur Hidayah Ibrahim, Ali Selamat |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2020-07-01
|
Series: | Frontiers in Public Health |
Subjects: | |
Online Access: | https://www.frontiersin.org/article/10.3389/fpubh.2020.00308/full |
Similar Items
-
Complexity Stage Model of the Medical Device Development Based on Economic Evaluation—MedDee
by: Petra Marešová, et al.
Published: (2020-02-01) -
Legislative and ethical aspects of introducing new technologies in medical care for senior citizens in developed countries
by: Kacetl J, et al.
Published: (2016-07-01) -
New Regulations on Medical Devices in Europe: Are They an Opportunity for Growth?
by: Petra Maresova, et al.
Published: (2020-03-01) -
Islamic Law and Women’s Rights in Indonesia: A Case of Regional Sharia Legislation
by: Hidayah, N.
Published: (2019) -
NEW PROPOSAL FOR EUROPEAN UNION REGULATIONS ON MEDICAL DEVICES AND IN VITRO DIAGNOSTIC MEDICAL DEVICES
by: Mariela Yaneva-Deliverska
Published: (2012-12-01)