Literature DB >> 9513003

Why certification of medical software would be useful?

J Forsström1.   

Abstract

Human drugs and medical devices have to be approved by the health authorities before they can enter the market. For medical software this is not needed. The main argument to resist all attempts to regulate medical software has been that it is impossible to guarantee that software is error-free. This is true of all software. However, in medical software the correctness of medical knowledge is at least as important as the correctness of the code itself. The medical contents of the software could usually be evaluated but the end-users do not have the time or possibilities to do so. The Internet makes it possible to provide commercial services designed by non-professionals. For health care, there are already several commercial services on the net. Since there is no quality assurance or regulation of medical software anyone can sell medical software on the net. Even if physicians were cautious enough not to use untested software, there is a possibility that patients do. In Finland, where over 10% of the population is using the Internet at least weekly, the problem is real. It is impossible to remove poor services from the net and therefore, it is essential to guide the users to use high quality services. The paper discusses different aspects of evaluation of medical software.

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Year:  1997        PMID: 9513003     DOI: 10.1016/s1386-5056(97)00098-1

Source DB:  PubMed          Journal:  Int J Med Inform        ISSN: 1386-5056            Impact factor:   4.046


  2 in total

1.  Verifying quality and safety in health informatics services.

Authors:  M Rigby; J Forsström; R Roberts; J Wyatt
Journal:  BMJ       Date:  2001-09-08

2.  Analysis of the Regulatory, Legal, and Medical Conditions for the Prescription of Mobile Health Applications in the United States, The European Union, and France.

Authors:  Parina Hassanaly; Jean Charles Dufour
Journal:  Med Devices (Auckl)       Date:  2021-11-24
  2 in total

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