The incorporation of a medical device into an IT network can introduce risks that may not have been addressed during the design and manufacture of the device. IEC 80001-1 is a lifecycle risk management standard which was developed to address these risks. This paper presents research which has been performed to date which has led to the development of a Process Reference Model (PRM) and Process Assessment Model (PAM) which can be used by Healthcare Delivery Organisations to assess themselves against IEC 80001-1. This paper also presents future work in this area which includes the development of an assessment method for IEC 80001-1 and the validation of the PRM, PAM and assessment method
Abstract. Increasingly medical devices are being designed to allow them to exchange information over...
Abstract: Medical devices are designed and produced subject to various standards. These standards ar...
IEC 80001-1:2010 [1] recognises that medical devices are incorporated into IT-networks to achieve d...
The incorporation of a medical device into an IT network can introduce risks that may not have bee...
peer-reviewedThe incorporation of a medical device into an IT network can introduce risks that may n...
The incorporation of a medical device into an IT network can introduce risks that may not have been ...
Medical devices are designed and produced subject to various standards. These standards are recogniz...
peer-reviewedIEC 80001-1 is a risk management standard that addresses the risks associated with the ...
peer-reviewedEfficiencies in patient care can be achieved through interoperability of medical device...
Increasingly medical devices are being designed to allow them to exchange information over an IT n...
IEC 80001-1 is a risk management standard that addresses the risks associated with the incorporati...
Medical Devices are widely used in patient care for both diagnosis and treatment purposes. Typically...
Efficiencies in patient care can be achieved through interoperability of medical devices. Patient sa...
Abstract. Increasingly medical devices are being designed to allow them to exchange information over...
Abstract: Medical devices are designed and produced subject to various standards. These standards ar...
IEC 80001-1:2010 [1] recognises that medical devices are incorporated into IT-networks to achieve d...
The incorporation of a medical device into an IT network can introduce risks that may not have bee...
peer-reviewedThe incorporation of a medical device into an IT network can introduce risks that may n...
The incorporation of a medical device into an IT network can introduce risks that may not have been ...
Medical devices are designed and produced subject to various standards. These standards are recogniz...
peer-reviewedIEC 80001-1 is a risk management standard that addresses the risks associated with the ...
peer-reviewedEfficiencies in patient care can be achieved through interoperability of medical device...
Increasingly medical devices are being designed to allow them to exchange information over an IT n...
IEC 80001-1 is a risk management standard that addresses the risks associated with the incorporati...
Medical Devices are widely used in patient care for both diagnosis and treatment purposes. Typically...
Efficiencies in patient care can be achieved through interoperability of medical devices. Patient sa...
Abstract. Increasingly medical devices are being designed to allow them to exchange information over...
Abstract: Medical devices are designed and produced subject to various standards. These standards ar...
IEC 80001-1:2010 [1] recognises that medical devices are incorporated into IT-networks to achieve d...