How to Develop and Implement a National Drug Policy - WHO Policy Perspectives on Medicines, No. 006, January 2003
(2003; 6 pages) [French] [Spanish] Voir le document au format PDF
Table des matières
Afficher le documentWhat is a national drug policy?
Afficher le documentObjectives of a national drug policy
Afficher le documentThe essential medicine concept is central to a national drug policy
Afficher le documentThe national drug policy process
Fermer ce répertoireKey components of a national drug policy
Afficher le documentSelection of essential medicines
Afficher le documentAffordability
Afficher le documentFinancing options
Afficher le documentSupply systems
Afficher le documentRegulation and quality assurance
Afficher le documentRational use
Afficher le documentResearch
Afficher le documentHuman resources development
Afficher le documentMonitoring and evaluation
Afficher le documentKey documents
 

Affordability

Affordable prices are an important prerequisite for ensuring access to essential medicines in the public and private sectors. This issue is important because resistance to well-known antibiotics, which are widely available as generic products, is increasing. New essential medicines for the treatment of some infectious diseases, such as malaria, tuberculosis and HIV/ AIDS, are often very costly. Key policy issues are:

• government commitment to ensuring access through increased affordability;

• for all medicines: removal or reduction of taxes and tariffs on essential medicines; control of distribution margins; pricing policy;

• for multi-source products (generic medicines and branded generics): promotion of competition through generic policies, generic substitution and good procurement practices;

• for single-source products: price negotiations, competition through price information and therapeutic substitution, and TRIPS-compliant measures such as compulsory licensing, “early workings” of patented medicines for generic manufacturers and parallel imports.

 

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Dernière mise à jour: le 3 mai 2013