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.

The symposium, which was inspired by the wonderful recent  PFC & Berkman Center Big Data conference,  featured enlightening speeches by former PFC fellows Nicholson Price on incentives for the development of black box personalized medicine and Jeff Skopek on privacy issues. In addition we were lucky to have Peter Yu speaking on “Big Data, Intellectual Property and Global Pandemics” and Michael J. Madison on Big Data and Commons Challenges”. The presentations and recordings of the session will soon be made available on our Center’s webpage.

Thanks everybody for your dedication, inspiration, great presentations and an exciting panel discussion.

“Legal Dimensions of Big Data in the Health and Life Sciences – From Intellectual Property Rights and Global Pandemics to Privacy and Ethics”

By PI Timo Minssen

“Our goal is to create a European Open Science Cloud to make science more efficient and productive and let millions of researchers share and analyze research data in a trusted environment across technologies, disciplines and borders”.                                   Carlos Moedas, EU Commissioner for Research, Science & Innovation

“The European Cloud Initiative will unlock the value of big data by providing world-class supercomputing capability, high-speed connectivity and leading-edge data and software services for science, industry and the public sector.”                                                         – Günther H. Oettinger, Commissioner for the Digital Economy and Society

Ladies and Gentleman,

I am very happy to welcome you to this seminar on the “Legal dimensions of Big Data in the Health and Life Sciences – From Intellectual Property Rights and Global Pandemics to Privacy and Ethics”.

The importance of this topic is not only emphasized by the above statements from EU Commissioners announcing the European Open Science Cloud initiative. Multiple factors indicate that “Big Data” will play a crucial role in the evolution of health care and the life sciences. The ongoing paradigm shift is fueled by rapid technical advances that have greatly enhanced the collection and analysis of information from multiple sources. In addition, U.S. and European authorities and public entities have in recent years developed public platforms and infrastructures that provide access to vast volumes of health-care knowledge, including clinical trials and selected patients data. Meanwhile, several private actors, such as pharmaceutical companies, health care providers, laboratories and insurance companies, have stored many years of R&D data into databases and digitalized their patient records. This trend is accompanied by recent initiatives and legislation that are increasing the transparency of various forms of data, such as clinical trials data.

As a result researchers, companies, patients and health care providers can now gain access to an enormously increased volume of personal and biological data. This information can be regarded as “big data,” i.e. not only because of the greater volume, but also for its’ increased variety, velocity, and veracity. Researchers can mine this data to identify the most effective treatments for particular conditions, to find 2nd and further medical uses, to detect patterns related to drug side effects or hospital readmissions, and gain other important information that can help patients and reduce costs. Although the data collections may be colossal and the quality of the data is often very diverse – depending on different database structures and technical characteristics- rapid technological advances and advanced algorithms have improved the ability of scientists to effectively analyze and use such data. It is expected that these developments will push the trend towards precision medicine and help us to address pressing problems, such as divergences in healthcare quality and ever-increasing healthcare costs. These vast prospects of Big Data and the gradual shift to more “personalized”, “open” and “transparent” innovation models highlight the significance of an effective and well-calibrated regulation, governance, and use of biological and personal data. At the same time, the ultimate goal of widespread data- sharing, as well as the risky and costly translation of Big Data science into safe and efficient “real world” applications raises multiple legal challenges relating to i.a. public-private research collaborations, data integrity, privacy, and ethics. In addition we will have to tackle pressing issues at the interface of intellectual property law, competition law, R&D incentives and commercialization.

As it will be discussed in the following sessions, we will have to ask ourselves and the decisions makers if the current legal frameworks need to be re-calibrated in specific areas to unlock the full potential of Big Data in the health and life sciences. Does our current toolbox have sufficiently flexible mechanisms in place or would we have to think in radically different ways and break new grounds?

With the new ESS- ERIC and Max IV facilities and other large international research infrastructures being developed in this region, such as the BBMRI-ERIC in biobanking, this is highly relevant for both the EU and for shaping national innovation policies and legal frameworks. Moreover, these new facilities need to carefully consider complex legal issues when drafting their operational policies and guidelines. What makes this a very delicate task is that, there seems to be much confusion about the availability, nature and the legal effects of a great variety of often overlapping rights and remedies among multiple stakeholders in Big Data science.

Against this background, we are of course delighted to have such a distinguished list of speakers among us. We will start out with a topic that concerns us all “Big Data, Intellectual Property and Global Pandemics!” Professor Yu, the stage is yours!

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This entry was posted in Generic Drugs, Global Health, Health Information Technology, Health Law Policy, Intellectual Property, International, Jeffrey Skopek, Malaria, Medical Privacy, Medical Safety, Mobile Health, Nicholson Price, Off-Label Use, Pharmaceuticals, Professional Regulation, Public Health, Research Funding, Scientific Evidence, Timo Minssen, Vaccines by Timo Minssen. Bookmark the permalink.

About Timo Minssen

Timo Minssen is Professor of Biotechnology Law specializing in legal aspects of biomedical innovation at the University of Copenhagen (UCPH), Centre for Information & Innovation Law (CIIR), Denmark. Before joining UCPH, Timo graduated from law school in Göttingen (Germany) in 2001 and was trained in the German court system from 2002-2003. He also passed the Swedish “juris licentiate” (LL.Lic.) and “juris doctor” exams (LL.D.) and holds two IP- and Biotech- related masters degrees from the Universities of Uppsala and Lund (Sweden). In addition he worked for a Life Science company and for various law firms in Sweden and Germany. From 2007-2009 Timo was a stipendiary at the Max Planck Institute for Intellectual Property and Competition Law in Munich. He was also responsible for a course in comparative patent law at the Chicago-Kent College of Law (USA) and worked for the European Patent Office. At Lund University he is engaged as a teacher at the Faculty of Law and in interdisciplinary epigenetics research at the Pufendorf Institute for Advanced Studies. At UCPH he is co-leading CIIR’s Copenhagen Biotech & Pharma Forum and teaches international classes for both students and pharma professionals in EU-, Competition-, and Pharmaceutical Law and IPR. Timo is a frequent speaker on a variety of topics and has published extensively in comparative US and European patent law, EU- and Competition Law. In 2013-14, he was a Visiting Scholar at Harvard Law School's Petrie-Flom Center and at the University of Oxford. In 2016 he will be Visiting Research Fellow at the University of Cambridge.

One thought on “Legal Dimensions of Big Data in the Health and Life Sciences

  1. Biotechnology has yielded public health, agricultural, and economic benefits as well as feeding back into the life sciences to improve development. Thus, improving healthy living through science and technology could be crucial.

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