This paper introduces the Multidisciplinary Assessment of Technology Centre for Healthcare (MATCH) and outlines the problem of integrating a user-centred approach for development of medical devices together with the information and communication technology environments in which they are increasingly required to operate. We highlight some of the regulatory requirements that are relevant to user needs consideration in medical device development. Finally, we reveal a range of limitations in the current practice of the medical device industry in the area of user needs capture, based on responses from interviews with MATCH’s industry partners
Background: It is well established that considering users is an important aspect of medical device d...
Abstract: High quality, well designed medical devices are necessary to provide safe and effective cl...
General methods of health technology assessment (HTA) are well-established, however their detailed ...
The healthcare industry is dependent upon the provision of well designed medical devices. To achiev...
Measuring and fulfilling user requirements during medical device development will result in successf...
Aims and Objectives: This research aims to suggest a concise framework to help in the better concep...
This thesis was submitted for the degree of Doctor of Philosophy and awarded by Brunel University.Ch...
Medical devices are used by a multiplicity of users and in a variety of environments. Manufacturers ...
High quality, well designed medical devices are necessary to provide safe and effective clinical car...
Health information technologies play an important role in exchange of information and coordination o...
This paper focuses on the challenges of meeting agency requirements as it pertains to the applicatio...
The medical device industry requires multi-disciplinary collaboration between researchers and physic...
Purpose – Medical device users are one of the principal stakeholders of medical device technologies....
Abstract Background Academic literature and international standards bodies suggest that user involve...
Copyright @ 2011 Money et al.Background: Academic literature and international standards bodies sugg...
Background: It is well established that considering users is an important aspect of medical device d...
Abstract: High quality, well designed medical devices are necessary to provide safe and effective cl...
General methods of health technology assessment (HTA) are well-established, however their detailed ...
The healthcare industry is dependent upon the provision of well designed medical devices. To achiev...
Measuring and fulfilling user requirements during medical device development will result in successf...
Aims and Objectives: This research aims to suggest a concise framework to help in the better concep...
This thesis was submitted for the degree of Doctor of Philosophy and awarded by Brunel University.Ch...
Medical devices are used by a multiplicity of users and in a variety of environments. Manufacturers ...
High quality, well designed medical devices are necessary to provide safe and effective clinical car...
Health information technologies play an important role in exchange of information and coordination o...
This paper focuses on the challenges of meeting agency requirements as it pertains to the applicatio...
The medical device industry requires multi-disciplinary collaboration between researchers and physic...
Purpose – Medical device users are one of the principal stakeholders of medical device technologies....
Abstract Background Academic literature and international standards bodies suggest that user involve...
Copyright @ 2011 Money et al.Background: Academic literature and international standards bodies sugg...
Background: It is well established that considering users is an important aspect of medical device d...
Abstract: High quality, well designed medical devices are necessary to provide safe and effective cl...
General methods of health technology assessment (HTA) are well-established, however their detailed ...