How to Develop a National Formulary Based on the WHO Model Formulary - A Practical Guide
(2004; 45 pages) View the PDF document
Table of Contents
View the documentAbbreviations
Open this folder and view contents1 INTRODUCTION
Open this folder and view contents2 OVERVIEW OF THE NATIONAL FORMULARY PROCESS
Open this folder and view contents3 DEVELOPING THE PRELIMINARY INFORMATION SECTION
Open this folder and view contents4 DEVELOPMENT OF THERAPEUTIC INFORMATION AND MONOGRAPHS USING THE WHO MODEL FORMULARY
Open this folder and view contents5 ADDITIONAL SOURCES OF INFORMATION
Close this folder6 DEVELOPING SPECIFIC INFORMATION SECTIONS
View the documentCreating locally important appendices
Open this folder and view contentsAdopting appendices from the WHO model formulary
Open this folder and view contentsWorking with a master document in Microsoft Word® to create a table of contents and index
Open this folder and view contents7 PRODUCTION, DISTRIBUTION AND IMPLEMENTATION
Open this folder and view contents8 EVALUATION
Open this folder and view contents9 REVIEW AND UPDATE
View the documentREFERENCES
 

6 DEVELOPING SPECIFIC INFORMATION SECTIONS

The appendices usually contain additional therapeutic, safety, pharmaceutical and administrative information (see Table 6.1) to supplement the monographs and general introductory texts. The information in this part of the formulary is frequently presented in a tabulated or summarized form and can also be illustrated with specific examples of local requirements.

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