Diagnostic Kits/Biotechnology and Intellectual Property Reinventing the Commons: Difference between revisions

From Commons Based Research
Jump to navigation Jump to search
No edit summary
No edit summary
Line 7: Line 7:
****"The original proposal for reform included a third party submission procedure for prior art,  a post- grant opposition process with two windows for launching opposition (one, immediately after issue and a second at any time later), limitations on the availability of preliminary injunctions, adoption of a  first-to-file rule (as opposed to the current first-to-invent rule), the requirement that all applications be published after 18 months (starting from the priority date) and a reinvigoration of the duty of candour." (page 18)
****"The original proposal for reform included a third party submission procedure for prior art,  a post- grant opposition process with two windows for launching opposition (one, immediately after issue and a second at any time later), limitations on the availability of preliminary injunctions, adoption of a  first-to-file rule (as opposed to the current first-to-invent rule), the requirement that all applications be published after 18 months (starting from the priority date) and a reinvigoration of the duty of candour." (page 18)
****These reforms meet fairly heavy resistance and have not been successful to date.  While these changes could effect patent law generally it is not clear than any of the proposed changes has any specific relevance to the field of diagnostic genetic kits.
****These reforms meet fairly heavy resistance and have not been successful to date.  While these changes could effect patent law generally it is not clear than any of the proposed changes has any specific relevance to the field of diagnostic genetic kits.
=Navigation=
[[Category:Diagnostic_Kits]]
[http://cyber.law.harvard.edu/commonsbasedresearch/Diagnostic_Kits#Resources DK Bibliography]<br>
[[Diagnostic_Kits]]<br>
[[Main Page]]

Revision as of 14:37, 4 May 2010

  • This report is a creation of the Intellectual Property Modeling Group (IPMG) based at the Centre for Intellectual Property Policy at McGill University. The intended audience is policy makers seeking to make informed decisions regarding the balancing of intellectual property rights within the area fo biotechnology.
  • Problems with intellectual property protection of biotechnological inventions
    • American, Canadian and Australian Issues
      • NO AMERICAN COMMENT
    • Proposed policies to address these concerns
      • proposed legislation to reform its patent law
        • "The original proposal for reform included a third party submission procedure for prior art, a post- grant opposition process with two windows for launching opposition (one, immediately after issue and a second at any time later), limitations on the availability of preliminary injunctions, adoption of a first-to-file rule (as opposed to the current first-to-invent rule), the requirement that all applications be published after 18 months (starting from the priority date) and a reinvigoration of the duty of candour." (page 18)
        • These reforms meet fairly heavy resistance and have not been successful to date. While these changes could effect patent law generally it is not clear than any of the proposed changes has any specific relevance to the field of diagnostic genetic kits.

Navigation

DK Bibliography
Diagnostic_Kits
Main Page