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
Open this folder and view contents6 DEVELOPING SPECIFIC INFORMATION SECTIONS
Open this folder and view contents7 PRODUCTION, DISTRIBUTION AND IMPLEMENTATION
Close this folder8 EVALUATION
View the documentEvaluation of the NF within the framework of existing monitoring and evaluation activities
View the documentHow to design the evaluation
Close this folderWhat to evaluate
View the documentPolicy, legal framework and management support
View the documentSelection
View the documentProcurement
View the documentDistribution of formulary
View the documentRational use
Open this folder and view contents9 REVIEW AND UPDATE
View the documentREFERENCES
 

What to evaluate

Specific questions related to the production, distribution and impact of the formulary can be categorized according to the medicine management cycle of selection, procurement, distribution and rational use, and can be supported by policies, a legal framework and management structures. The following examples of indicators and questions are listed together with these assessment points.

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