Eye on the Ball. Medicine Regulation – Not IP Enforcement – Can Best Deliver Quality Medicines
(2011; 51 pages)
Abstract

In the interests of individual patient safety and public health in general, the capacity of developing-country DRAs to regulate medicines should be strengthened. A commitment to providing reliable and affordable medicines, together with the provision of universal health services and medicines, should be embedded in national policies and strategies to improve health-care infrastructure. The capacity of DRAs to properly enforce medicines regulations must be assured...


 
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