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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
 

3.5 Local production

Goal: to consider, and support if appropriate, development of efficient local production of essential drugs of good quality, safety and efficacy, relevant to national needs and resources.

Objectives:

1. To create an environment conducive to the establishment of increased national capacity for the production of essential drugs

2. To ensure that local production follows recommended procedures, ie. current Good Manufacturing Practice (cGMP), and statutory requirements


Strategies:

1. Establish a system of incentives for the local manufacture of essential drugs (eg. tax incentives, tender preference, reduced import tariffs, reduced rates for electricity and water consumption)

2. Institute regular and systematic inspection of premises and processes to ensure full adherence to licensing requirements and current Good Manufacturing Practice (cGMP)

3. Improve local pharmaceutical technical capacity by encouraging and assisting in the training of sufficient numbers of staff in pharmaceutical production techniques, quality assurance and cGMP.

4. Institute a system of monitoring and support supervision to ensure maintenance of required standards.

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