The fast-track registration policy of the South African (SA) National Department of Health (DoH) allows for rapid registration of new medicines of public health importance and of all medicines on the Essential Medicines List, most of which are generics. No limit is placed on the number of generic brands of a medicine that can be submitted for fast-track registration. This, together with resource constraints at the regulator, may delay access to important new medicines, new fixed-dose combinations of critical medicines or affordable versions of biological medicines (biosimilars). One reason for not limiting the number of fast-track generic applications was to promote price competition among generic brands. We found this not to be valid, sinc...
There have been multiple reforms in South Africa to conserve resources including policies to enhance...
There have been multiple reforms in South Africa to conserve resources including policies to enhance...
Background: The aims of this study were to compare the overall regulatory review timelines achieved ...
A thesis submitted to the Faculty of Health Sciences, University of the Witwatersrand, in fulfilment...
Introduction: Due to the increase in healthcare costs, generic medicines have been adopted for used ...
Introduction: Due to the increase in healthcare costs, generic medicines have been adopted for used ...
Background: Regulatory authorities register medicines for patients to access them within a reasonabl...
Background: This research focuses on pharmaceutical competition in South Africa where concurrent pri...
Background: This research focuses on pharmaceutical competition in South Africa where concurrent pri...
Research Report in partial fulfillment of MSc (Med) Pharmaceutical Affairs Department of Pharmacy a...
Background: Sub-Saharan Africa is going through an epidemiological transition, including an impressi...
A research report submitted to the Faculty of Health Sciences, University of Witwatersrand, in parti...
Background: Sub-Saharan Africa is going through an epidemiological transition, including an impressi...
Background: Sub-Saharan Africa is going through an epidemiological transition, including an impressi...
Background: Sub-Saharan Africa is going through an epidemiological transition, including an impressi...
There have been multiple reforms in South Africa to conserve resources including policies to enhance...
There have been multiple reforms in South Africa to conserve resources including policies to enhance...
Background: The aims of this study were to compare the overall regulatory review timelines achieved ...
A thesis submitted to the Faculty of Health Sciences, University of the Witwatersrand, in fulfilment...
Introduction: Due to the increase in healthcare costs, generic medicines have been adopted for used ...
Introduction: Due to the increase in healthcare costs, generic medicines have been adopted for used ...
Background: Regulatory authorities register medicines for patients to access them within a reasonabl...
Background: This research focuses on pharmaceutical competition in South Africa where concurrent pri...
Background: This research focuses on pharmaceutical competition in South Africa where concurrent pri...
Research Report in partial fulfillment of MSc (Med) Pharmaceutical Affairs Department of Pharmacy a...
Background: Sub-Saharan Africa is going through an epidemiological transition, including an impressi...
A research report submitted to the Faculty of Health Sciences, University of Witwatersrand, in parti...
Background: Sub-Saharan Africa is going through an epidemiological transition, including an impressi...
Background: Sub-Saharan Africa is going through an epidemiological transition, including an impressi...
Background: Sub-Saharan Africa is going through an epidemiological transition, including an impressi...
There have been multiple reforms in South Africa to conserve resources including policies to enhance...
There have been multiple reforms in South Africa to conserve resources including policies to enhance...
Background: The aims of this study were to compare the overall regulatory review timelines achieved ...