Protection of innovation in the pharmaceutical industry has traditionally been realised through protection of inventions via patents. However, in the European Union regulatory exclusivities restricting market entry of generic products confer tailored, industry specific protection for final, marketable products. This paper retraces the protection conferred by the different forms of exclusivity and assesses them in the light of recent transparency policies of the European Medicines Agency. The purpose of the paper is to argue for rethinking the role of regulatory data as a key tool of innovation policy and for refocusing the attention from patents to the existing regulatory framework. After detailed assessment of the exclusivity regime, the p...
69-88Data-exclusivity is one of the most controversial issues in the current discussion on pharmaceu...
International audienceGovernments are trying to stimulate drug R&D for unmet health needs with publi...
The European Union (EU) has instituted internal and external measures aimed at protecting and enforc...
Abstract After lengthening the duration of patents to twenty years in 1984, the pharmaceutical indus...
After lengthening the duration of patents to twenty years in 1984, the pharmaceutical industry has t...
Abstract The challenge of providing access to high-priced patented medicines is a global problem aff...
This Article is set in the background of the consequences of the WTO’s prescriptions on patenting of...
This article reexamines the sources of exclusivity for drugs, considers their limitations, and evalu...
Data exclusivity is temporary exclusive user right on the clinical data that need to be submitted to...
Development of innovative drugs is a lengthy, risky and expensive enterprise, and the research-based...
There has been a general downgrading of patent from its touted original has position of being the un...
Pharmaceutical firms typically enjoy market exclusivity for new drugs from concurrent protection of ...
Congress is current considering legislation that would create a regulatory pathway for follow-on bio...
Since the adoption of the WTO-TRIPS Agreement in 1994, there has been significant controversy over t...
Resume - Supplementary Protection Certificates for Medicinal Products Nowadays, the pharmaceutical i...
69-88Data-exclusivity is one of the most controversial issues in the current discussion on pharmaceu...
International audienceGovernments are trying to stimulate drug R&D for unmet health needs with publi...
The European Union (EU) has instituted internal and external measures aimed at protecting and enforc...
Abstract After lengthening the duration of patents to twenty years in 1984, the pharmaceutical indus...
After lengthening the duration of patents to twenty years in 1984, the pharmaceutical industry has t...
Abstract The challenge of providing access to high-priced patented medicines is a global problem aff...
This Article is set in the background of the consequences of the WTO’s prescriptions on patenting of...
This article reexamines the sources of exclusivity for drugs, considers their limitations, and evalu...
Data exclusivity is temporary exclusive user right on the clinical data that need to be submitted to...
Development of innovative drugs is a lengthy, risky and expensive enterprise, and the research-based...
There has been a general downgrading of patent from its touted original has position of being the un...
Pharmaceutical firms typically enjoy market exclusivity for new drugs from concurrent protection of ...
Congress is current considering legislation that would create a regulatory pathway for follow-on bio...
Since the adoption of the WTO-TRIPS Agreement in 1994, there has been significant controversy over t...
Resume - Supplementary Protection Certificates for Medicinal Products Nowadays, the pharmaceutical i...
69-88Data-exclusivity is one of the most controversial issues in the current discussion on pharmaceu...
International audienceGovernments are trying to stimulate drug R&D for unmet health needs with publi...
The European Union (EU) has instituted internal and external measures aimed at protecting and enforc...