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
Close this folder3 DEVELOPING THE PRELIMINARY INFORMATION SECTION
View the documentDeveloping locally relevant introductory information
Open this folder and view contentsGeneral entries at the front of a national formulary
Close this folderAdditional information at the front of the national formulary
View the documentInstructions on how to use the formulary
View the documentGlossary
View the documentPolicies and procedures of the national formulary and national formulary committee
View the documentNational policies and regulations
View the documentList of changes
View the documentAdapting the “General advice to prescribers” section of the WHO model formulary
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
Open this folder and view contents6 DEVELOPING SPECIFIC INFORMATION SECTIONS
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
 

List of changes

Lists of changes can alert the reader to changes in revised editions of the NF. They should be presented in a clear way, with a brief explanation or reference when necessary. Potential changes that may be listed are:

- significant changes in therapeutic information;
- deletion or addition of drugs;
- discontinuation or addition of individual preparations; and
- changes in dose or classification of existing entries.

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