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close this bookUganda National Drug Policy (WHO; 2002; 45 pages)
View the documentForeword
View the documentPreface
View the documentIntroduction
View the documentMembers of the MoH Task Force on Drug Management
View the documentNational Drug Policy
View the document1. Pharmaceutical legislation and regulation
View the document2. Drug selection
close this folder3. Drug supply system (quantification, procurement, storage, distribution)
View the document3.1 Quantification
View the document3.2 Procurement (including donations)
View the document3.3 Storage and inventory control
View the document3.4 Distribution
View the document3.5 Local production
View the document3.6 Quality assurance
View the document3.7 Disposal of expired or otherwise unwanted drugs and medical supplies
Open this folder and view contents4. Rational drug use and drug information
Open this folder and view contents5. Drug financing and pricing
View the document6. Traditional medicines
View the document7. Human resource development
View the document8. Research and development
View the document9. Technical co-operation
View the document10. Monitoring and evaluation
 

3.1 Quantification

Goal: to establish and maintain a reliable system with appropriate mechanisms for regular and accurate quantification of essential drug needs at all levels of the health system.

Objectives:

1. To improve the availability and reliability of required quantification data
2. To enhance the capacity to carry out quantification at each level of the health system
3. To improve the ability to correctly utilise the data
4. To avoid wastage and drug expiry caused by over-estimation of requirements


Strategies:

1. Promote collaboration with relevant partners (eg. members of the district health team, national drug procurement agency, national drug regulatory agency) to establish and maintain a reliable drug management information system (DMIS) and health management information system (HMIS) which will ensure the ready availability of accurate morbidity and drug consumption data required for drug quantification purposes and the regular and timely feedback of useful information to the partners

2. Develop and distribute quantification guidelines for each level.

3. Ensure the necessary quantification capacity at all levels by training sufficient relevant staff in record-keeping and quantification methodology and by providing adequate monitoring and supervision of the processes involved

4. Systematically collect and analyse the relevant data

5. Ensure that periodic and regular quantification is carried out at all levels.

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