Intellectual Property

  • Read more: Legal Dimensions of Big Data in the Health and Life Sciences

    Legal Dimensions of Big Data in the Health and Life Sciences

    By Timo Minssen Please find below my welcome speech at last-weeks mini-symposium on “Legal dimensions of Big Data in the Health and Life Sciences – From Intellectual Property Rights and Global Pandemics to Privacy and Ethics at the University of Copenhagen (UCPH).  The event was organized by our Global Genes –Local Concerns project, with support from the UCPH Excellence Programme for Interdisciplinary Research.…

  • Read more: Divided Infringement in Patent Law and the Doctor-Patient Relationship

    Divided Infringement in Patent Law and the Doctor-Patient Relationship

    By Rachel Sachs Regular readers of this blog (hi, Mom) will recall that I often think and write about the interaction between the divided infringement doctrine in patent law and medical method patents of various kinds.  In previous posts, I’ve written about the Federal Circuit’s efforts to assign liability for divided infringement of method patents…

  • Read more: Separating sheep from goats- a European view on the patent eligibility of biomedical diagnostic methods

    Separating sheep from goats- a European view on the patent eligibility of biomedical diagnostic methods

    By Timo Minssen New publication on the patentability of biomedical diagnostics out: Abstract: This brief comment complements Dan Burk’s excellent paper ( Dolly and Alice, J Law and the Biosciences (2015), 1–21, doi:10.1093/jlb/lsv042 ) by providing a very brief summary of the European approach regarding patents on medical diagnostic methods. This serves as the basis for…

  • Read more: Amicus brief in Sequenom v. Ariosa: Why the U.S. Supreme Court should grant the petition for a writ of certiorari

    Amicus brief in Sequenom v. Ariosa: Why the U.S. Supreme Court should grant the petition for a writ of certiorari

    By Timo Minssen I am happy to announce that on April 20th the New York attorney Robert M. Schwartz and I have filed an amicus brief at the US Supreme Court with Berkeley-based Andrew J. Dhuey as Counsel of Record. The brief, which was signed by 10 prominent  European and Australian Law Professors as amici curiae, adds a…

  • Read more: One Patent Law, Two Economic Sectors: Is The One-Size-Fits-All Patent Law Still Workable?

    One Patent Law, Two Economic Sectors: Is The One-Size-Fits-All Patent Law Still Workable?

    This new post by Claire Laporte appears on the Health Affairs Blog as part of a series stemming from the Fourth Annual Health Law Year in P/Review event held at Harvard Law School on Friday, January 29, 2016. Ever since the first patent was issued in 1790, the United States has had a single patent law to protect inventions in all fields.…

  • Read more: Sequenom vs. Ariosa and international approaches to the patent eligibility of biomedical innovation

    Sequenom vs. Ariosa and international approaches to the patent eligibility of biomedical innovation

    By Timo Minssen With a potential petition for writ of certiorari in the Sequenom v. Ariosa case approaching, it appears as if the US Supreme Court  will once again have to consider crucial patent eligibility questions with a great significance for biomedical innovation and diagnostic methods. The claims at issue (see U.S. Patent No. 6,258,540 ) are directed to methods of genetic testing by detecting and…

  • Read more: Stem cell patenting on the other side of the pond

    Stem cell patenting on the other side of the pond

    By Timo Minssen We are pleased to announce a new publication in the International Review of Intellectual Property and Competition Law (IIC). Our paper analyzes new case law in European stem cell patenting and compares these developments with the US situation and International treaties. Further information and an abstract is available below: Authors: Ana Nordberg & Timo Minssen, University of Copenhagen, Centre…

  • Read more: Evolving Industry Structures in Biosimilar Development

    Evolving Industry Structures in Biosimilar Development

    By Rachel Sachs Yesterday, I had the privilege to moderate a fantastic event here at the Petrie-Flom Center on Assessing the Viability of FDA’s Biosimilars Pathway.  Bringing together expert panelists from legal practice (Donald R. Ware, Partner, Foley Hoag LLP), industry (Konstantinos Andrikopoulos, Lead IP Counsel, Manufacturing, Biogen, Inc.), and academia (W. Nicholson Price II,…

  • Read more: March-In Rights Alone Won’t Solve Our Drug Pricing Problems

    March-In Rights Alone Won’t Solve Our Drug Pricing Problems

    By Rachel Sachs On Monday, a group of over 50 members of Congress sent a letter urging the Department of Health and Human Services (HHS) and the National Institutes of Health (NIH) to use a little-known statutory provision to take action against high drug prices.  Their goal is laudable, and HHS and the NIH should…

  • Read more: FDA Releases Report Detailing Problematic Laboratory-Developed Tests

    FDA Releases Report Detailing Problematic Laboratory-Developed Tests

    By Rachel Sachs Last week, the FDA issued a report presenting 20 case studies of laboratory-developed tests (LDTs) that have or may have harmed patients, in support of its ongoing efforts to impose greater regulatory oversight on LDTs.  The report came just before yet another House Energy & Commerce Committee hearing on the issue, and…