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Pharmaceuticals and the Internet Drug Regulatory Authorities' Perspective - Joint NLN-WHI Workshop, 24-25 September 2001
(2002; 80 pages) View the PDF document
Table of Contents
View the documentExecutive Summary
View the documentOverview of activities by the World Health Organization - Dr Lembit Rägo
View the documentOverview of activities by the Nordic Council on Medicines - Dr Ola Westbye
Open this folder and view contentsCountry Experiences
View the documentThe Danish Consumer Council - Ms Margrethe Nielsen
View the documentSwedish Industry Association - Dr Håkan Mandahl
View the documentIntroduction to discussion points - Dr Lembit Rägo
View the documentQuality aspects - Dr Ola Westbye
View the documentPilot study on drug regulatory web sites: Current status and future challenges - Ms Elodie Jambert
View the documentThe WHO model web site for drug regulatory authorities - Dr Lembit Rägo, Ms Elodie Jambert, Mr Jorg Hetzke
View the documentConcluding discussion
Open this folder and view contentsAnnexes
View the documentReferences
View the documentBack cover
 

Concluding discussion

Medical Products and the Internet

The feedback on this publication was that the tone is negative, in that the emphasis is more on what not to do rather than what should be done. There is a great deal of poor-quality information on the Internet, but sources of reliable information should be highlighted and users should be assisted in their search for such sources.

WHO will consider the need to review this document and to give good examples, and will try to meet the needs.

Information

Patients, consumers, and health professionals want to know what the good web sites on health information are.

With respect to medical information available on the Internet, DRAs should provide more information to a wider spectrum of audiences. The main target audiences should be more clearly defined and should be able to obtain specific information relating to their respective areas of interest.

WHO Model Web Site

The WHO Model Web Site was well received so far as concept and purpose are concerned. The following suggestions were made.

• A minimum set of information that is related to the core functions of a DRA should be defined, i.e., information that is uniquely available from DRAs should be made accessible - in so far as confidentiality rules and data security allow.

• The model web site should be pre-configured with WHO guideline information and basic data.

• The model web site could be provided with a standard installation of the WHO Model Drug Registration Software.

WHO should revise its current version of the model web site and then start deploying a new version based on the suggestions made by the audience.

Ideally, WHO could assist a selected number of interested countries in establishing a DRA web site based on the revised WHO model. In a further step, these DRA-initiated model web sites could then be validated by a panel of users from different audiences.

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Last updated: April 24, 2012