Starting or Strengthening a Drug Bulletin - A Practical Manual
(2005; 165 pages) View the PDF document
Table of Contents
View the documentPreface
View the documentHow the manual was produced
View the documentAbout ISDB
View the documentExecutive summary
Open this folder and view contents1. Introduction
Open this folder and view contents2. Rational use of medicines
Open this folder and view contents3. What are drug bulletins?
Open this folder and view contents4. Defining aims, target and type of bulletin
Open this folder and view contents5. Planning resources
Open this folder and view contents6. Planning bulletin production: schedules and timing
Close this folder7. The editorial process
View the document7.1 Outline of the editorial process
Close this folder7.2 Editing a drug bulletin
View the document7.2.1 Editorial independence
View the document7.2.2 Strong and sustained editorial policy and a committed team
View the document7.2.3 Selecting topics for articles
View the document7.2.4 Using and adapting existing material
View the document7.2.5 Planning a bulletin issue
Open this folder and view contents7.3 Writing bulletin articles
Open this folder and view contents7.4 Reviewing the article
View the document7.5. Rewriting the article
View the document7.6 Final checks
Open this folder and view contents7.7 Follow-up after publication
View the document7.8 References
Open this folder and view contents8. Reviewing a new drug: is it a therapeutic advance?
Open this folder and view contentsAnnexe to Chapter 8: Evaluating harm
Open this folder and view contents9. Design and production
Open this folder and view contents10. Dissemination
Open this folder and view contents11. Organizational and legal issues
Open this folder and view contents12. Evaluating quality and usefulness
Open this folder and view contents13. Partnership and collaboration
Open this folder and view contents14. Keeping records and creating a memory
Open this folder and view contentsAppendix: Electronic sources of information
 

7.2.4 Using and adapting existing material

Editing a good quality original article for a drug bulletin takes time. To save time, energy and resources, the exchange and adaptation of good-quality articles among bulletins may be very useful for topics that are common to different countries with similar health care conditions.

Before beginning to write an original article, it is worth checking to see whether another bulletin has already produced an article on the same topic. An article may be reproduced, translated, summarised or adapted. This avoids unnecessary waste of resources, especially for new bulletins or bulletins with few people involved. It also allows editors to concentrate their energy on local topics requiring original work. Using existing material can also help well-established bulletins to show their readers that health professionals in one country can benefit from outside experience. An article from another country or an external source may also add weight to a controversial position (see Box 7.2).

Box 7.2 Mutual support among bulletins

Many examples from ISDB show how bulletins can support each other:

• During one of the first misleading public promotional campaigns in France (the campaign on sumatriptan), la revue Prescrire contributed to a more objective appraisal of the evidence not only through its own articles, but also by publishing summaries of articles on the drug from Geneesmiddelenbulletin, Drug and Therapeutics Bulletin, Informazioni sui Farmaci, and Pharma Selecta.

TheNetwork in Pakistan was able to raise questions about why chlormezanone was still on the market in Pakistan when other countries had withdrawn the drug, referring to articles in bulletins of countries that had taken regulatory action.

• The bulletin of the Swedish Medical Products Agency, Information fran Läkemedelsverket, and la revue Prescrire have produced a collaborative study comparing their judgement on the added therapeutic value of newly marketed drugs. The fact that these very different bulletins often reach the same conclusions gives weight to their assessments.4

It is sometimes possible to collaborate with local or national institutions and to reproduce their materials if the information supports rational drug use. If foreign material is used, careful adaptation is obviously essential. In some cases this may not be possible, for example, if the health care systems of the two countries are too different.

Specific rules govern the reproduction of existing materials (see also Section 11.5 of Chapter 11):

• Copyright rules governing periodicals, textbooks, formularies, recommendations and guidelines, as well as the publications of organizations such as WHO, non-governmental organizations, scientific societies, etc. may vary. To avoid unpleasant surprises, it is important to contact the publisher and ask about conditions for reproduction.

• Always state the source of any reprinted material, including tables, drawings and any other graphic material.


Most organizations allow reproduction of their materials and are often pleased to be able to help bulletins.

to previous section
to next section
 
 
The WHO Essential Medicines and Health Products Information Portal was designed and is maintained by Human Info NGO. Last updated: June 25, 2014