Canada’s Patented Medicines (Notice Of Compliance) Regulations fail to achieve the intended purpose of balancing innovation with timely generic market entry. An examination of the inefficiencies created by the Canadian regulations reveals that key features of U.S. pharmaceutical law should be adopted to improve the disjointed regulatory system that impedes generic competition. Specifically, the regulations should be amended to consolidate multiple proceedings into one cause of action that evaluates patent validity. An economic incentive to challenge weak patents should also be introduced in Canada. These features encourage competition without deterring pharmaceutical research and development because only patents that are not truly inven...
This article is an analysis of case law pertaining to whether scientific research in the lead-up to ...
The table of contents for this item can be shared with the requester. The requester may then choose ...
Three important aspects of the Canadian pharmaceutical industry-viz. compulsory licence, price contr...
Canada’s Patented Medicines (Notice Of Compliance) Regulations fail to achieve the intended purpose ...
Abstract Background In order to comply with the provi...
Canada\u27s linkage regime for pharmaceuticals, modeled after the originating U.S. Hatch-Waxman reg...
The table of contents for this item can be shared with the requester. The requester may then choose ...
The current COVID-19 pandemic has highlighted the significance of the export-oriented compulsory lic...
This article analyzes the Canadian court case of Eli Lilly v. Novopharm and the utility doctrine i...
A fundamental purpose of patent law is to encourage the development of new inventions by granting to...
Biologics and biosimilars represent the promise for more effective treatments of many diseases. Inte...
When generic drugs seek FDA approval, the pharmaceutical company files an Abbreviated New Drug Appli...
In order to market and sell a new pharmaceutical drug in Canada, the Minister of Health requires the...
With its Bill C-56 to amend the Patent Act andthe Food and Drugs Act in order to ease patentrestrict...
In 1994, the members of the World Trade Organisation (WTO) adopted the Agreement on Trade-Related As...
This article is an analysis of case law pertaining to whether scientific research in the lead-up to ...
The table of contents for this item can be shared with the requester. The requester may then choose ...
Three important aspects of the Canadian pharmaceutical industry-viz. compulsory licence, price contr...
Canada’s Patented Medicines (Notice Of Compliance) Regulations fail to achieve the intended purpose ...
Abstract Background In order to comply with the provi...
Canada\u27s linkage regime for pharmaceuticals, modeled after the originating U.S. Hatch-Waxman reg...
The table of contents for this item can be shared with the requester. The requester may then choose ...
The current COVID-19 pandemic has highlighted the significance of the export-oriented compulsory lic...
This article analyzes the Canadian court case of Eli Lilly v. Novopharm and the utility doctrine i...
A fundamental purpose of patent law is to encourage the development of new inventions by granting to...
Biologics and biosimilars represent the promise for more effective treatments of many diseases. Inte...
When generic drugs seek FDA approval, the pharmaceutical company files an Abbreviated New Drug Appli...
In order to market and sell a new pharmaceutical drug in Canada, the Minister of Health requires the...
With its Bill C-56 to amend the Patent Act andthe Food and Drugs Act in order to ease patentrestrict...
In 1994, the members of the World Trade Organisation (WTO) adopted the Agreement on Trade-Related As...
This article is an analysis of case law pertaining to whether scientific research in the lead-up to ...
The table of contents for this item can be shared with the requester. The requester may then choose ...
Three important aspects of the Canadian pharmaceutical industry-viz. compulsory licence, price contr...