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Front-end web development is the development of the graphical user interface of a website through the use of HTML, CSS, and JavaScript so users can view and interact with that website. [1] [2] [3] [4]
The Freescale Healthcare AFE reference platform is a highly integrated HW/SW development platform, that helps reduce system cost, board size and complexity.
Front-end development is the process of designing and implementing the user interface (UI) and user experience (UX) of a web application. It involves creating visually appealing and interactive elements that users interact with directly. The primary technologies and concepts associated with front-end development include:
In software development, frontend refers to the presentation layer that users interact with, while backend involves the data management and processing behind the scenes. In the client–server model, the client is usually considered the frontend, handling user-facing tasks, and the server is the backend, managing data and logic.
Front-end web development – the practice of converting data to a graphical interface, through the use of HTML, CSS, and JavaScript, so that users can view and interact with that data. HTML (HyperText Markup Language) (*.html) CSS (Cascading Style Sheets) (*.css) CSS framework; JavaScript (*.js) Package managers for JavaScript
NextGen Healthcare, Inc. is an American software and services company headquartered in Atlanta, Georgia.The company develops and sells electronic health record (EHR) software and practice management systems to the healthcare industry, as part of a range of software, services and analytics solutions for medical and dental practices.
Health information technology (HIT) is "the application of information processing involving both computer hardware and software that deals with the storage, retrieval, sharing, and use of health care information, health data, and knowledge for communication and decision making". [8]
The development of the ISO 9000-3 standard [9] as well as the European Medical Devices Directive in 1993 [1] helped bring some harmonization of existing laws with medical devices and their associated software, and the addition of IEC 62304 in 2006 further cemented how medical device software should be developed and tested. [11]