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Clinical trials raise a variety of benefit-cost and cost-effectiveness considerations. To date, these considerations have received minimal attention from persons performing trials. Analysis of the benefit-cost aspects of a trial should shed additional light on, or add a new dimension to, the...
Persistent link: https://www.econbiz.de/10013000671
). This Article adopts Thomas Kuhn's paradigm theory to explain the active function of licensing law in purifying and …
Persistent link: https://www.econbiz.de/10013000778
There are ongoing debates regarding the nature and scope of intellectual property protection, if any, which clinical trial data should receive in terms of Article 39 of the TRIPS Agreement.These debates however occur in the international and bilateral contexts thus excluding key stakeholders in...
Persistent link: https://www.econbiz.de/10013000924
In this paper we document a process of price convergence in the European market for pharmaceutical products and relate it to access to innovative medicines in individual countries. The EU is a peculiar case study, where free circulation of goods coexists with pricing policies designed and...
Persistent link: https://www.econbiz.de/10013001124
employ novel data and exploit the timing and geographic location of a crackdown on legal suppliers of pharmaceuticals in …
Persistent link: https://www.econbiz.de/10013001270
Background Although medical oncologists can have an important role in controlling the cost of cancer treatment, there is little information about their attitudes toward the cost of cancer treatment and the impact of cost on their treatment recommendations, especially in low- and middle-income...
Persistent link: https://www.econbiz.de/10013002206
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