Prof. Timo Minssen

København, Region Hovedstaden, Danmark Kontaktoplysninger
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Law Professor & advisor, striving for more sustainable & responsible innovation…

Aktivitet

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Erfaring og uddannelse

  • Petrie-Flom Centre for Health Law Policy, Biotechnology, and Bioethics at Harvard Law School, US

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Udgivelser

  • Intellectual Property Rights,Standards and Data Exchange in System Biology

    Biotechnology Journal

    Standardization and data exchange in SysBio may result in challenges and opportunities related to IPRs. The aim of this article is to raise awareness on these issues within the SysBio scientific community and to stimulate exploration of different strategies for dealing with IPRs in order to optimize access to and use of valuable research results.

    Andre forfattere
    Se udgivelse
  • Synthetic biology and intellectual property rights: Six recommendations

    Biotechnology Journal

    On 26th November 2013, the Danish Agency for Science, Technology and Innovation organized an expert meeting on “Synthetic Biology & Intellectual Property Rights” in Copenhagen sponsored by the European Research Area Network in Synthetic Biology (ERASynBio). The meeting brought together ten experts from different countries with a variety of professional backgrounds to discuss emerging challenges and opportunities at the interface of synthetic biology and intellectual property rights. The aim of…

    On 26th November 2013, the Danish Agency for Science, Technology and Innovation organized an expert meeting on “Synthetic Biology & Intellectual Property Rights” in Copenhagen sponsored by the European Research Area Network in Synthetic Biology (ERASynBio). The meeting brought together ten experts from different countries with a variety of professional backgrounds to discuss emerging challenges and opportunities at the interface of synthetic biology and intellectual property rights. The aim of this article is to provide a summary of the major issues and recommendations discussed during the meeting.

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  • Standardization, IPRs and Open Innovation in Synthetic Biology

    Edward Elgar

    Our paper describes IP and standardization aspects of Synthetic Biology in order to discuss them in the context of the “open innovation” discourse. We concentrate on describing the technology and identifying areas of particular relevance. Ultimately we also sketch out open questions and potential solutions requiring further research.

    Section 1 commences with a brief introduction to the fascinating science of SB and a description of recent technological advances and applications. This…

    Our paper describes IP and standardization aspects of Synthetic Biology in order to discuss them in the context of the “open innovation” discourse. We concentrate on describing the technology and identifying areas of particular relevance. Ultimately we also sketch out open questions and potential solutions requiring further research.

    Section 1 commences with a brief introduction to the fascinating science of SB and a description of recent technological advances and applications. This will lead us to section 2, in which we will address standard setting efforts in SB, as well as the relevance and governance of various IPRs for specific SB standards. This provides the basis for section 3, in which we debate problematic issues and summarize our conclusions.

    Keywords: standardization, open innovation, synthetic biology, intellectual property rights

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  • A Sequel to US Patent Eligibility in the Wake of Bilski v. Kappos: Business as Usual in an Age of New Technologies?

    30 Biotech. L. Rep., 57 (2011)

    Andre forfattere
  • Life after Myriad: the uncertain future of patenting biomedical innovation and personalised medicine in an international context

    I.P.Q. 2015, 3 189-241 (July 2015)

    On June 13, 2013, the U.S. Supreme Court decided the Myriad gene patent case. In a unanimous judgment the Court held that patent claims directed to isolated genomic DNA are – in contrast to cDNA - identical to the naturally occurring sequence and thus not patent eligible “products of nature”. It appears therefore that for a new biological composition of matter to be patent eligible, it must not be identical to the naturally occurring biological composition. This decision affects all isolated…

    On June 13, 2013, the U.S. Supreme Court decided the Myriad gene patent case. In a unanimous judgment the Court held that patent claims directed to isolated genomic DNA are – in contrast to cDNA - identical to the naturally occurring sequence and thus not patent eligible “products of nature”. It appears therefore that for a new biological composition of matter to be patent eligible, it must not be identical to the naturally occurring biological composition. This decision affects all isolated "products of nature", including genes, gene fragments, and other naturally occurring nucleotide sequences, as well as naturally occurring amino acid sequences, including peptides, ligands, and proteins. Consequently, Myriad has a severe impact on many patent portfolios. Although Myriad does not directly affect the patentability of cDNA or sufficiently modified compounds, and the most recent USPTO guidance provides hints on how the new eligibility standard can be met, it is still not entirely clear how much modification is required to render a molecule sufficiently distinct from naturally occurring counterparts. Moreover, when combined with the US Supreme Court decisions in Prometheus and Alice, Myriad may affect method claims which depend upon unmodified biological materials. The USPTO guidance, however, still leaves much uncertainty over the patentability of such methods and diagnostics. The substantial impact of these decisions on the biomedical sector and personalized medicine, as well the methodology used by the generalist Supreme Court in reversing a specialized CAFC judgment is particularly interesting from a comparative perspective. This paper analyses and discusses these U.S. developments, and compares them with the situation in Australia and in the EU

    Andre forfattere
  • Myriad reloaded and ready for the next round? The Association for Molecular Pathology v USPTO 689 F.3d 1303 (Fed. Cir. 2012)

    3 Queen Mary J. Intell. Prop. 70 (2013)


    Andre forfattere
  • Standing on Shaky Ground- US patent-eligibility of isolated DNA and genetic diagnostics after AMP v. USPTO - Part IV

    3 Queen Mary J. Intell. Prop. 118 (2013)

    Andre forfattere
  • US Patent Eligibility in the Wake of Bilski v. Kappos: Business as Usual in an Age of New Technologies?

    30 Biotech. L. Rep., 3 (2011)

    Andre forfattere

Projekter

  • Additive Manufacturing and Innovation: Technical, Economic, Legal, and Policy Related Aspects of Rising Technologies (AdManI)

    Joint project between Hanken (Dep of Accounting and Commercial law), the Aalto University (Department of Engineering Design and Production) and the University of Helsinki (School of law) ), conducted in co-operation with the IPR University Centre and the Universities of Copenhagen, Bournemouth, and Pforzheim.

    This research project is an international collaborative study that strives for groundbreaking results on fundamental questions related to intellectual property (IP) law, rising…

    Joint project between Hanken (Dep of Accounting and Commercial law), the Aalto University (Department of Engineering Design and Production) and the University of Helsinki (School of law) ), conducted in co-operation with the IPR University Centre and the Universities of Copenhagen, Bournemouth, and Pforzheim.

    This research project is an international collaborative study that strives for groundbreaking results on fundamental questions related to intellectual property (IP) law, rising technologies (such as additive manufacturing), innovation, and policies. The AdManI project will run during 2015-2016 and will be financed by Tekes.

    Andre skabere
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  • Copenhagen Summer University: Course for executives in Pharmaceutical Law & Policy

    Once again I will be the course director of the 3rd edition of the “Copenhagen Summer School” for pharma professionals. The course will be held from August 18th -22nd at the Frederiksberg campus of the University of Copenhagen. It covers the hottest regulatory and scientific topics in the field from a comparative US/European viewpoint including a special day focusing on emerging markets in Asia. I will teach a variety of lectures with case studies and will be joined by a team of expert…

    Once again I will be the course director of the 3rd edition of the “Copenhagen Summer School” for pharma professionals. The course will be held from August 18th -22nd at the Frederiksberg campus of the University of Copenhagen. It covers the hottest regulatory and scientific topics in the field from a comparative US/European viewpoint including a special day focusing on emerging markets in Asia. I will teach a variety of lectures with case studies and will be joined by a team of expert colleagues from medicine authorities, IP Law firms, major pharmaceutical companies, researchers, and the former White House Director of international IP.

    Se projekt
  • BioSYNergy: Synthetic Biology - towards a Bio-Based Society

    coPI, WP leader and member of the steering committee, 1 PhD student and 1 PostDoc

    Andre skabere
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  • Counterfeit Medicines

    Counterfeiting medicines have become an enormous industry. Although counterfeit medicines may look genuine, there are often no or very little active ingredient in them. Furthermore, they are often produced under conditions unsuitable for manufacturing medicines and without respect for intellectual property rights and human life.

    The problem is well-known in countries with weak quality assurance systems where stories of counterfeit medicines reaching patients in large numbers are routine.…

    Counterfeiting medicines have become an enormous industry. Although counterfeit medicines may look genuine, there are often no or very little active ingredient in them. Furthermore, they are often produced under conditions unsuitable for manufacturing medicines and without respect for intellectual property rights and human life.

    The problem is well-known in countries with weak quality assurance systems where stories of counterfeit medicines reaching patients in large numbers are routine. However, several high profile cases in Europe and the United States have made it apparent that also the Western countries need to react in order to protect their supply chains.

    Through our research we study;

    • the distribution of counterfeit medicines in countries without strong regulatory bodies

    • how highly regulated supply chains attempt to block the distribution of counterfeit medicines

    • the development and implementation of new EU legislation

    • how private and public stakeholders work together to combat counterfeit medicines

    The research on counterfeit medicines is done in collaboration with Centre for Information and Innovation Law at the Faculty of Law.

    Andre skabere
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  • ERASynBio Initiative

    – nu

    DEVELOPMENT AND COORDINATION OF SYNTHETIC BIOLOGY IN THE EUROPEAN RESEARCH AREA

    The ERASynBio Initiative

    ERASynBio is an initiative of international funding agencies working together to promote the robust development of Synthetic Biology and to structure and coordinate national efforts and funding programs. The network was created in 2012 and funded as an ERA-Net by the European Commission under FP7 until 2014. From 2015 onwards, ERASynBio will operate as a self-sustainable…

    DEVELOPMENT AND COORDINATION OF SYNTHETIC BIOLOGY IN THE EUROPEAN RESEARCH AREA

    The ERASynBio Initiative

    ERASynBio is an initiative of international funding agencies working together to promote the robust development of Synthetic Biology and to structure and coordinate national efforts and funding programs. The network was created in 2012 and funded as an ERA-Net by the European Commission under FP7 until 2014. From 2015 onwards, ERASynBio will operate as a self-sustainable initiative (i.e. without the financial support of the EC), with most ERA-Net partners continuing their collaboration in the next years.

    Along with the 2 joint calls, several supporting measures were initiated by ERASynBio in order to support the development of high quality Synthetic Biology research. One major effort was the development of a Strategic Vision accompanied by a series of targeted recommendations designed to empower national and international funding organizations, policy bodies and other stakeholders.

    It is the aim of the ERASynBio initiative to further support joint activities that focus on transnational coordination, capacity building, sharing resources and facilities, and - last but not least - joint calls for proposals in the field of synthetic biology.

    Coordinator

    Dr. Marion Karrasch-Bott
    Phone: +49 2461 61 6245
    Mail: m.karrasch@fz-juelich.de

    Se projekt
  • ERASysAPP - ERA-Net for Systems Biology Applications

    – nu

    The main objective of the ERANET proposal Systems Biology Applications - ERASysAPP (app = application = translational systems biology) is to promote multidimensional and complementary European systems biology projects, programmes and research initiatives on a number of selected research topics. Inter alia, ERASysAPP will initiate, execute and monitor a number of joint transnational calls on systems biology research projects with a particular focus on applications - or in other words so called…

    The main objective of the ERANET proposal Systems Biology Applications - ERASysAPP (app = application = translational systems biology) is to promote multidimensional and complementary European systems biology projects, programmes and research initiatives on a number of selected research topics. Inter alia, ERASysAPP will initiate, execute and monitor a number of joint transnational calls on systems biology research projects with a particular focus on applications - or in other words so called translational systems biology research approaches (application-oriented and/or industry-relevant). The joint call proposals and their respective attention will be on applied aspects of complex biological processes in microorganisms, plants and animals. As common feature, all addressed proposal topics will tackle biological and physiological processes of common interest in the field of life sciences and biotechnology.
    In order to reach our ambitious goals, ERASysAPP has been outlined to initiate novel activities and impulses for SB in the ERA. Taking past successful developments and achievements into account, ERASysAPP will be able to continue and build on work, which has been performed by the previously funded successful ERANET on SB, ERASysBio and its spin-offs ERASysBio+, SysMo and SysMO2 (www.erasysbio.net). This is advantageous, since it allows for the efficient use of past experiences and tangible results of ERASysBio and will guarantee for maximum synergistic effects. Although building on the improvements of ERASysBio, ERASysAPP will provide a bundle of novel aspects, ideas, activities and sustainable new features to push SB towards new challenges and horizons. Apart from setting up joint transnational calls and giving impulses for industry to apply more SB approaches, ERASysAPP will focus on horizontal topics such as improved data management and sharing, training and networking with national, transnational, and EU SB initiatives as well as programmes outside the ERA

    Se projekt
  • Copenhagen Summer University - Pharmaceutical Law & Policy

    Gave presentation about regulation of approval of biosimilars and determination of interchangeability/substitution of biosimilars in Europe at Summer University program aimed at industry and scientific community participants by the University of Copenhagen.

    Andre skabere
    Se projekt

Udmærkelser og priser

  • Jorcks Foundation Research Prize

    Jorcks Foundation

  • King Oscar Prize for best dissertation

    Swedish Royal Court & Lund University

    Prize for the best dissertation at Lund University.

  • Awapatent Research Prize

    Awapatent

Sprog

  • German

    Modersmåls- eller tosprogsfærdighed

  • English

    Komplet professionel færdighed

  • Norwegian

    Begrænset praktisk færdighed

  • Russian

    Elementær færdighed

  • French

    Elementær færdighed

  • Swedish

    Modersmåls- eller tosprogsfærdighed

  • Danish

    Begrænset praktisk færdighed

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