Full recordShow full item record
Abstract[This item is a preserved copy and is not necessarily the most recent version. To view the current item, visit http://www.jmir.org/2000/2/e9/ ] The Internet is changing how people receive health information and health care. All who use the Internet for health-related purposes must join together to create an environment of trusted relationships to assure high quality information and services; protect privacy; and enhance the value of the Internet for both consumers and providers of health information, products, and services. The goal of the e-Health Code of Ethics is to ensure that people worldwide can confidently and with full understanding of known risks realise the potential of the Internet in managing their own health and the health of those in their care. The final e-Health Code of Ethics, presented in this paper, has been prepared as a result of the "e-Health Ethics Summit," which convened in Washington DC on 31 January 2000 - 2 February 2000. The summit, organized by the Internet Healthcare Coalition and hosted by the World Health Organisation/Pan-American Health Organisation (WHO/PAHO), was attended by a panel of about 50 invited experts from all over the world and produced the foundation for a draft code, which was released 18 February  for an online public consultation period which ended on 14 April 2000. The final Washington e-Health Code of Ethics sets forth guiding principles under eight main headings: candor; honesty; quality; informed consent; privacy; professionalism in online health care; responsible partnering; and accountability. Note: Abstract, keywords, acknowledgements and references have been added by the editor and are not part of the final Code.
Helga Rippen, Ahmad Risk. e-Health Code of Ethics (May 24). J Med Internet Res 2000;2(2):e9 <URL: http://www.jmir.org/2000/2/e9/>
Copyright/LicenseCopyright (cc) Retained by author(s) under a Creative Commons License: http://creativecommons.org/licenses/by/2.0/