Filter by input type
Select all
News
Pages
Events
Filter by category
Select all
AI ANALYTICS
Mobile Apps and Internet of Things
Advancement of science
big data
Connected communities
Coronavirus
Courses and training
DIAGNOSIS
Initial Editorial
Editorials
A world in the cloud
Events
Infographics
Artificial Intelligence and Science
IoT Apps
News
Digital platforms
Social networks
Review of scientific publications
Course Summary
Synopsis of essay
Overview of reference frames
Synopsis of recent publications
Use of Digital Platforms
Filter by input type
Select all
News
Pages
Events
Filter by category
Select all
AI ANALYTICS
Mobile Apps and Internet of Things
Advancement of science
big data
Connected communities
Coronavirus
Courses and training
DIAGNOSIS
Initial Editorial
Editorials
A world in the cloud
Events
Infographics
Artificial Intelligence and Science
IoT Apps
News
Digital platforms
Social networks
Review of scientific publications
Course Summary
Synopsis of essay
Overview of reference frames
Synopsis of recent publications
Use of Digital Platforms
Oxford Global Guidance the digital platform for understanding medical device regulation

The University of Oxford created a digital platform aimed at personnel working in the area of medical devices and their development, to learn about and understand the regulations of various devices.

The University of Oxford, through its Natural Interaction Laboratory (NIL) in the department of Engineering Science, has created a web-based digital tool aimed at people working around medical device development. The tool was funded by the Engineering and Physical Sciences Research Council (EPSRC) of the United Kingdom and the European Institute of Innovation and Technology (EIT), a European Union (EU) institution.

Oxford Global Guidance is a digital tool to facilitate and streamline understanding of how medical device regulations apply to new products or products under development. On their website, they indicate that the tool was launched earlier than expected, as due to the COVID-19 pandemic, they sought to drive a functional platform for medical equipment personnel to navigate and learn about medical device regulations and requirements, specifically in the EU.

The platform is divided in four steps, first the online support for the description of the device; subsequently, the platform presents a questionnaire to evaluate whether or not it is a medical device according to EU regulations; the third step, the classification involves another questionnaire to find out to which classification the device belongs according to EU MDR and IVDR regulations; finally the result, will provide a more extensive overview for decision making with experts in healthcare institutions or for the improvement of the device in its development process.

This process takes at least 20 minutes and is offered free of charge through a basic registration via an email address. It is currently in a process of continuous improvement, to add new features and better navigation.

Outstanding news

News by country

Share

Digital Health in the world

  • — Science Brief: Omicron (B.1.1.529) Variant/CDC updates
    See more
  • —Coronavirus resource center/Johns Hopkins
    See more
  • — Epidemiological tracing of COVID-19 contacts / Johns Hopkins Course
    See more
  • — SARS-CoV-2 infection behavior / FCS calculator
    See more
  • — Omicron SARS-CoV-2 variant: a new chapter in the COVID-19 pandemic/ Article The Lancet
    See more
  • —Genomic Epidemiology Tracker/GISAID
    See more
  • — Mexican Genomic Surveillance Consortium
    See more
Secured By miniOrange