MONITORINGTHESAFETYOFapproved medical prod-uctsisofvitalpublichealthimportance, given that in clinical practice suchmedical products areoftenused innumbers fargreaterand inpatientpopulationsmorediverse than when studied in premarket evaluations and clinical trials.1-6 Within the broad range ofmedical products, implantable medicaldevicesrepresenthigh-riskprod-ucts that are uniquely challenging to monitorbecause there is little consensus regarding themostappropriatemethods to account for the complex interactions amongdevices,medications,patients,and implanting physicians. In addition, the lackofuniquemedicaldevice identifier
This reviews the transition of remote monitoring of patients with cardiac electronic implantable dev...
Background. The optimum approach for infectious complication surveillance for cardiac implantable el...
SummaryBackgroundA programme for quality assurance and prevention of infection risk during implantat...
MONITORINGTHESAFETYOFapproved medical prod-uctsisofvitalpublichealthimportance, given that in clinic...
Background—Postmarket medical device surveillance in the United States depends largely on voluntary ...
The development and introduction of new medical deviceshave radically changed the practice of medici...
textabstractRecent safety issues involving non-active implantable medical devices (NAIMDs) have high...
The availability of new therapies over the past 2decades has dramatically changed the practice ofmed...
Introduction The lack of a terminology to compare medical devices together with the arbitrary and o...
Cardiovascular implantable electronic devices (CIEDs) have expanded in number and complexity since t...
BACKGROUND The process of assuring the safety of medical devices is constrained by reliance on volun...
The number of patients implanted with car-diovascular electronic devices (CIED) like im-plantable de...
Thesis (S.M.)--Harvard-MIT Division of Health Sciences and Technology, 2006.Vita.Includes bibliograp...
AbstractCardiac implantable electronic devices are increasing in prevalence and functionality. Post-...
Background: Machine learning methods may complement traditional analytic methods for medical device ...
This reviews the transition of remote monitoring of patients with cardiac electronic implantable dev...
Background. The optimum approach for infectious complication surveillance for cardiac implantable el...
SummaryBackgroundA programme for quality assurance and prevention of infection risk during implantat...
MONITORINGTHESAFETYOFapproved medical prod-uctsisofvitalpublichealthimportance, given that in clinic...
Background—Postmarket medical device surveillance in the United States depends largely on voluntary ...
The development and introduction of new medical deviceshave radically changed the practice of medici...
textabstractRecent safety issues involving non-active implantable medical devices (NAIMDs) have high...
The availability of new therapies over the past 2decades has dramatically changed the practice ofmed...
Introduction The lack of a terminology to compare medical devices together with the arbitrary and o...
Cardiovascular implantable electronic devices (CIEDs) have expanded in number and complexity since t...
BACKGROUND The process of assuring the safety of medical devices is constrained by reliance on volun...
The number of patients implanted with car-diovascular electronic devices (CIED) like im-plantable de...
Thesis (S.M.)--Harvard-MIT Division of Health Sciences and Technology, 2006.Vita.Includes bibliograp...
AbstractCardiac implantable electronic devices are increasing in prevalence and functionality. Post-...
Background: Machine learning methods may complement traditional analytic methods for medical device ...
This reviews the transition of remote monitoring of patients with cardiac electronic implantable dev...
Background. The optimum approach for infectious complication surveillance for cardiac implantable el...
SummaryBackgroundA programme for quality assurance and prevention of infection risk during implantat...