Article | REF: TE7504 V2

International Regulation and Standardisation in bodies of e-Health equipments

Author: Daniel BATTU

Publication date: February 10, 2020

You do not have access to this resource.
Click here to request your free trial access!

Already subscribed? Log in!


Overview

Français

ABSTRACT

Managing natural disasters and major epidemics could be complex if global regulations and standards had not been prepared. The availability of new electronic health equipment required an overall effort to rationalize. This article summarizes the role and relationships of various agencies involved in defining these materials and in the related regulations. The World Health Organization brings its specificity to the many bodies for standardizing these materials. The aspects of medical data exchange, as well as drug standards and regulations, are briefly discussed.

Read this article from a comprehensive knowledge base, updated and supplemented with articles reviewed by scientific committees.

Read the article

AUTHOR

  • Daniel BATTU: Honorary Telecommunications Consultant (ECTI), Rennes, France

 INTRODUCTION

Information and communication technologies (ICT) are helping to support the development and management of conventional medicine. They offer an excellent opportunity to rationalize the organization of care by medical specialty on a national scale, and to demonstrate the economic profitability of the most appropriate structures and methods.

The World Health Organization (WHO), supported by the United Nations and a number of charitable foundations, defines research programs, coordinates terminology and the use of regulatory standards and principles. It presents evidence-based intervention options, with technical support for the poorest countries.

Thanks to the close collaboration established between the many standardization bodies set up around the world, analysis and research work on human health and physical well-being is progressing rapidly. This work brings together the medical and ICT worlds, while respecting generally accepted moral rules and good practices relating to transaction security. Transfers of personal health information are carried out in complete confidentiality. The manufacture of pharmaceutical products is governed by strict standards that international regulations attempt to maintain in all regions of the world.

In every country, ICTs can help reduce healthcare costs while improving the quality of healthcare systems. By describing the landscape of regulatory and standardization bodies involved, this article attempts to objectively indicate the division of responsibilities currently assumed at national and international levels. Global or national management of the healthcare field is probably the most important human activity, and the continuous evolution of the technologies involved means that precise and constant adaptation is essential.

You do not have access to this resource.

Exclusive to subscribers. 97% yet to be discovered!

You do not have access to this resource.
Click here to request your free trial access!

Already subscribed? Log in!


The Ultimate Scientific and Technical Reference

A Comprehensive Knowledge Base, with over 1,200 authors and 100 scientific advisors
+ More than 10,000 articles and 1,000 how-to sheets, over 800 new or updated articles every year
From design to prototyping, right through to industrialization, the reference for securing the development of your industrial projects

This article is included in

Healthcare technologies

This offer includes:

Knowledge Base

Updated and enriched with articles validated by our scientific committees

Services

A set of exclusive tools to complement the resources

Practical Path

Operational and didactic, to guarantee the acquisition of transversal skills

Doc & Quiz

Interactive articles with quizzes, for constructive reading

Subscribe now!

Ongoing reading
Regulation and standardization of electronic equipment in the healthcare sector
Outline