How Open Science Helps Researchers Succeed Erin Mckiernan National Autonomous University of Mexico
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Discover the History of Science the History of the Royal Society
Discover the history of science The history of the Royal Society Founded in 1660, the Royal Society is the Boyle and John Wilkins, the group national academy of science in the UK, soon received royal approval, and from made up of a Fellowship of approximately 1663 it would be known as ‘The Royal 1,600 of the world’s most eminent Society of London for Improving Natural scientists. Throughout our history, we Knowledge’. have played a part in some of the most life-changing discoveries, and remain The early years of the Society saw dedicated to recognising, supporting, revolutionary advancements in the and promoting excellence in science. conduct and communication of science. Hooke’s Micrographia and the first The origins of the Royal Society lie in issue of Philosophical Transactions a group of people who began meeting were published in 1665. Philosophical in the mid-1640s to discuss the new Transactions, which established the philosophy of promoting knowledge of important concepts of scientific priority the natural world through observation and peer review, is now the oldest and experiment, which we now call continuously published science journal science. The very first ‘learned society’ in the world. meeting on 28 November 1660 followed a lecture at Gresham College To find out more, visit: by Christopher Wren. Joined by other royalsociety.org/about-us/history leading polymaths including Robert Image: Illustrations showing microscopic views of seaweed and rosemary from Micrographia,by Robert Hooke, 1665. The Royal Society’s journal of the history of science. Editor: Professor Anna Marie Roos, University of Lincoln, UK. -
Revamping Federal Climate Science Recommendations for the Next President of the United States
GETTY SHIPING IMAGES/LIU Revamping Federal Climate Science Recommendations for the Next President of the United States By John Podesta, Bidisha Bhattacharyya, and Bianca Majumder December 2020 WWW.AMERICANPROGRESS.ORG Contents 1 Introduction and Summary 4 Recommendations to restore scientific integrity across the government 9 Recommendations for rebuilding the federal climate science workforce 13 Recommendations to coordinate climate science in the White House and across the federal government 19 Recommendations to define interagency climate science research and data priorities 31 Recommendations for prioritizing adaptation and resilience 34 Recommendations to promote international coordination on climate science 40 Conclusion 41 About the authors 41 Acknowledgments 44 Appendix: References and further reading 46 Endnotes Introduction and summary The United States has been the global leader in climate science for decades. Unfortunately, progress has slowed—and in some cases, even moved backward— over the past four years, with the Trump administration dismantling core elements of the federal climate science apparatus. As the country and the planet head toward an increasingly unstable climate, the U.S. government needs to get back to the business of being the preeminent source of trusted applied science that supports climate change mitigation and adaptation decision-making of governments and civilian stakeholders. The science is clear: To avoid the worst impacts of climate change, the United States and the world must take aggressive action to decarbonize all sectors of the global economy, protect the Earth’s natural systems, and limit warming to 1.5 degrees Celsius above preindustrial levels. This means achieving net-zero greenhouse gas emissions globally by no later than 2050 and ensuring an equitable and just transition to a clean energy economy. -
Joint Statement on Public Disclosure of Results from Clinical Trials
Joint statement on public disclosure of results from clinical trials Signatories on 18 May 2017 Indian Council of Medical Research Research Council of Norway UK Medical Research Council Médecins Sans Frontières Epicentre CEPI PATH Institut Pasteur Bill and Melinda Gates Foundation Wellcome Trust Introduction The current 2013 Declaration of Helsinki states that “Every research study involving human subjects must be registered in a publicly accessible database before recruitment of the first subject.” and that “Researchers have a duty to make publicly available the results of their research .... Negative and inconclusive as well as positive results must be published or otherwise made publicly available”. In addition to the ethical imperative, poor allocation of resources for product development and financing of available interventions, and suboptimal regulatory and public health recommendations may occur where decisions are based on only a subset of all completed clinical trials. The signatories of this joint statement affirm that the prospective registration and timely public disclosure of results from all clinical trials is of critical scientific and ethical importance. Furthermore timely results disclosure reduces waste in research, increases value and efficiency in use of funds and reduces reporting bias, which should lead to better decision-making in health. Within 12 months of becoming a signatory of this statement, we each pledge to develop and implement a policy with mandated timeframes for prospective registration and public disclosure of the results of clinical trials that we fund, co-fund, sponsor or support. We each agree to monitor registration and endorse the development of systems to monitor results reporting on an ongoing basis. -
Institutional and Individual Influences on Scientists' Data Sharing Behaviors
Syracuse University SURFACE School of Information Studies - Dissertations School of Information Studies (iSchool) 2013 Institutional and Individual Influences on Scientists' Data Sharing Behaviors Youngseek Kim Follow this and additional works at: https://surface.syr.edu/it_etd Part of the Library and Information Science Commons Recommended Citation Kim, Youngseek, "Institutional and Individual Influences on Scientists' Data Sharing Behaviors" (2013). School of Information Studies - Dissertations. 85. https://surface.syr.edu/it_etd/85 This Dissertation is brought to you for free and open access by the School of Information Studies (iSchool) at SURFACE. It has been accepted for inclusion in School of Information Studies - Dissertations by an authorized administrator of SURFACE. For more information, please contact [email protected]. Abstract Institutional and Individual Influences on Scientists’ Data Sharing Behaviors by Youngseek Kim In modern research activities, scientific data sharing is essential, especially in terms of data-intensive science and scholarly communication. Scientific communities are making ongoing endeavors to promote scientific data sharing. Currently, however, data sharing is not always well-deployed throughout diverse science and engineering disciplines. Disciplinary traditions, organizational barriers, lack of technological infrastructure, and individual perceptions often contribute to limit scientists from sharing their data. Since scientists’ data sharing practices are embedded in their respective disciplinary contexts, -
Transparency in the Time of Constant Change
PhUSE 2014 Paper RG02 Transparency in the Time of Constant Change Todd Case, Biogen Idec, Cambridge MA, USA ABSTRACT The time has come, after years of hard work, to submit your application to the regulatory agency for review and possible approval! What a relief to be able to finally hand off all of your hard work and, wait a minute, ensure that all data can be reproducible?!? While CDISC has been widely adopted and its SDTM and AdAM models widely implemented, there is still the need to understand the process of ensuring that all the data is a reflection of how it was originally collected, which in some cases can be very challenging. This paper will discuss some more trending ways of both creating and presenting data in ways that ensure it is consumable and can be understood not only for analysis/submission purposes but also that post-approval it is transparent and that everyone who has a vested stake can review the data in an appropriate way. INTRODUCTION With the publication of Bad Pharma: How Medicine is Broken , and How We Can Fix it, by Dr. Ben Goldacre in 2013 a bright spotlight was shone on the data behind/supporting clinical trials. A large part of his thesis is that pharmaceutical companies exaggerate the efficacy of successful trials and that, in addition to drug companies, regulators , physicians (who are educated by the drug companies) and even patient groups have failed to protect us. Another rather striking revelation was that a clinical trial with positive results is twice more likely to be published than one with negative results (although it should be noted that this specifically is related to results – the protocol is always provided). -
Patents, Partnerships, and the Pre-Competitive Collaboration Myth in Pharmaceutical Innovation
Patents, Partnerships, and the Pre-Competitive Collaboration Myth in Pharmaceutical Innovation Liza S. Vertinsky* Public-private partnerships offer a promising alternative paradigm for pharmaceutical innovation in complex disease areas where there are both strong commercial interests and significant public need. They have the potential to reduce the tremendous waste associated with duplicative unsuccessful drug development efforts and to encourage the sharing of knowledge essential to accelerate pharmaceutical innovation. Patents threaten the potential of partnership strategies, however, by making it harder to sustain robust systems of knowledge sharing. Policymakers have tried to avoid this problem by focusing partnership strategies on areas deemed to be pre-competitive — areas of collaboration without competition and typically also without patents. This Article suggests that the current pre-competitive approach to partnership strategies in pharmaceutical innovation is fundamentally flawed for two reasons. First, it ignores the competitive market pressures that both shape what is deemed to be pre-competitive and fuel tensions * Copyright © 2015 Liza S. Vertinsky. Associate Professor of Law, Emory University School of Law. Many thanks to Timothy Holbrook, Timothy Terrell, Yaniv Heled, Cynthia Ho, Kevin Outterson, and Michael Carroll, as well as Sean O’Connor, Roger Ford, Dan Burk, Mark McKenna, and other participants of the Yale Innovation Beyond IP conference 2014; Arti Rai, Jerome Reichman, Katherine Strandburg, Brett Frischmann, Michael Madison, Peter Lee, Margaret Chon, Sonali Shah, and the other participants in the Medical Commons Workshop at NYU in May 2014 and the 2nd Thematic Conference on the Knowledge Commons at NYU in September 2014; participants in the summer workshop at Georgia State College of Law in July 2014; participants of the Emory Faculty Colloquium; Simon Stern, Abraham Drassinower, Margaret J. -
OPEN SCIENCE' an Essay on Patronage, Reputation and Common Agency Contracting in the Scientific Revolution
This work is distributed as a Discussion Paper by the STANFORD INSTITUTE FOR ECONOMIC POLICY RESEARCH SIEPR Discussion Paper No. 06-38 THE HISTORICAL ORIGINS OF 'OPEN SCIENCE' An Essay on Patronage, Reputation and Common Agency Contracting in the Scientific Revolution By Paul A. David Stanford University & the University of Oxford December 2007 Stanford Institute for Economic Policy Research Stanford University Stanford, CA 94305 (650) 725-1874 The Stanford Institute for Economic Policy Research at Stanford University supports research bearing on economic and public policy issues. The SIEPR Discussion Paper Series reports on research and policy analysis conducted by researchers affiliated with the Institute. Working papers in this series reflect the views of the authors and not necessarily those of the Stanford Institute for Economic Policy Research or Stanford University. THE HISTORICAL ORIGINS OF ‘OPEN SCIENCE’ An Essay on Patronage, Reputation and Common Agency Contracting in the Scientific Revolution By Paul A. David Stanford University & the University of Oxford [email protected] or [email protected] First version: March 2000 Second version: August 2004 This version: December 2007 SUMMARY This essay examines the economics of patronage in the production of knowledge and its influence upon the historical formation of key elements in the ethos and organizational structure of publicly funded open science. The emergence during the late sixteenth and early seventeenth centuries of the idea and practice of “open science" was a distinctive and vital organizational aspect of the Scientific Revolution. It represented a break from the previously dominant ethos of secrecy in the pursuit of Nature’s Secrets, to a new set of norms, incentives, and organizational structures that reinforced scientific researchers' commitments to rapid disclosure of new knowledge. -
Report on Transparency and Registration in Clinical Research In
Transparency and Registration in Clinical Research in the Nordic Countries By the Nordic Trial Alliance Working Group on Transparency and Registration Transparency and Registration in Clinical Research in the Nordic Countries Nordic Trial Alliance NordForsk Stensberggata 25 NO-0170 Oslo www.nta.nordforsk.org Design: jnd.no Printed by: 07 Group ISSN 1504-8640 ER JØM KE IL T M 2 4 9 1 7 3 Trykksak Transparency and Registration in Clinical Research in the Nordic Countries By the Nordic Trial Alliance Working Group on Transparency and Registration 1 Table of Contents Preface 4 The Nordic Trial Alliance Working Group on Transparency and Registration 6 Conflicts of Interest 7 Abbreviations 8 1. Executive summary 16 2. Background 20 3. Introduction to transparency 30 4. International policies and regulations impacting the future of transparency 36 4.1 The Declaration of Helsinki 36 4.2 The Food and Drug Administration Amendments Act of 2007 36 4.3 The European Clinical Research Infrastructures Network (ECRIN) 37 4.4 European Medicines Agency 37 4.5 Horizon 2020 38 4.6 Regulation on clinical trials on medicinal product for human use 39 4.7 EU Regulation for data protection 40 5. Arguments in favour of and against transparency 44 5.1 Arguments in favour 44 5.2 Arguments against 49 6. Does publication of trial protocols or trial results in registers impede journal publications? 54 7. Registries and repositories 58 2 8. Status of the Nordic countries 62 8.1 Current national procedures for public, prospective registration and reporting of clinical -
Histories of Medical Lobbying’
‘Histories of medical lobbying’ The lobbying of government ministers by medical professionals is a live issue. In Britain and around the world medical practitioners have become active in the pursuit of legislative change. In the UK, the AllTrials campaign co-founded by the physician-researcher Ben Goldacre continues to exert pressure on parliamentarians in a bid to force greater transparency in the publication of clinical trial results. Meanwhile, the California Medical Association advocates the legalisation of the recreational use of marijuana, and doctors in Australia refuse to release child refugees from hospital into detention centres damaging to their mental health. It was precisely the lobbying of medical humanitarians such as Médecins sans Frontières in France that effected a change in the law there in 1998, permitting undocumented immigrants with life-threatening conditions to remain in the country for medical treatment. Each of these examples represents an organised attempt on the part of medical professionals to change government policy on matters related to public health – in other words, lobbying. Yet a recent announcement by the UK cabinet office suggests that henceforth recipients of public funding will be banned from directly lobbying government ministers in the hope of changing public policy. When questioned in parliament David Cameron stated that charities should be devoting themselves to ‘good causes’ rather than ‘lobbying ministers’. Unless some qualification is forthcoming, medical researchers too will be proscribed from carrying out such activity. This insinuates that lobbying is in some way outside the proper remit of researchers, medical or otherwise. Yet even a cursory glance at the history of the medical profession’s engagement with public health reveals a longstanding and significant engagement with the political process. -
SENSE ABOUT SCIENCE 14A Clerkenwell Green London EC1R 0DP T 020 7490 9590
SENSE ABOUT SCIENCE 14A Clerkenwell Green London EC1R 0DP T 020 7490 9590 Registered Charity No. 1146170 Company No. 6771027 Registered in England and Wales Response to House of Commons Science and Technology Select Committee inquiry on research integrity 10th March 2017 Sense about Science is an independent charity that challenges the misrepresentation of science and scientific evidence in public life. We advocate for openness and honesty about research findings, and work to ensure the public interest in sound science and evidence is represented and recognised in public discussion and policy making. Sense about Science runs the AllTrials campaign which calls for all past and present clinical trials to be registered and their full methods and summary results reported. The AllTrials campaign is providing a separate submission for this inquiry. However there are two other areas under the terms of this inquiry that we would like to bring the committee’s attention. A single, publicly searchable database of all government-commissioned research In June 2015 Sense about Science began an inquiry into whether the government is reporting the policy research it commissions, following a spate of accusations of suppression of inconvenient results. Led by the former Appeal Court judge, Rt Hon Sir Stephen Sedley, its report Missing Evidence was published in June 2016.1 The inquiry revealed widespread confusion in the way research commissioned by government is handled, both internally and with the public: • There are significant differences in the way departments report and record research; • 11 government departments were unable to provide a list of research they have commissioned; • Of these, seven said that they did not hold that information centrally and it would be too costly to gather. -
Improving Medicines for Children in Canada
IMPROVING MEDICINES FOR CHILDREN IN CANADA The Expert Panel on Therapeutic Products for Infants, Children, and Youth Science Advice in the Public Interest IMPROVING MEDICINES FOR CHILDREN IN CANADA The Expert Panel on Therapeutic Products for Infants, Children, and Youth ii Improving Medicines for Children in Canada THE COUNCIL OF CANADIAN ACADEMIES 180 Elgin Street, Suite 1401, Ottawa, ON, Canada K2P 2K3 Notice: The project that is the subject of this report was undertaken with the approval of the Board of Governors of the Council of Canadian Academies (the Council). Board members are drawn from the Royal Society of Canada (RSC), the Canadian Academy of Engineering (CAE), and the Canadian Academy of Health Sciences (CAHS), as well as from the general public. The members of the expert panel responsible for the report were selected by the Council for their special competencies and with regard for appropriate balance. This report was prepared for the Government of Canada in response to a request from the Minister of Health. Any opinions, findings, or conclusions expressed in this publication are those of the authors, the Expert Panel on Therapeutic Products for Infants, Children, and Youth, and do not necessarily represent the views of their organizations of affiliation or employment. Library and Archives Canada Cataloguing in Publication Library and Archives Canada Cataloguing in Publication Improving medicines for children in Canada / The Expert Panel on Therapeutic Products for Infants, Children, and Youth. Issued also in French under title: Améliorer les médicaments pour enfants au Canada. Includes bibliographical references and index. Issued in print and electronic formats. -
The NSB a History in Highlights 1950-2000
The National Science Board A History in Highlights 1950-2000 NATIONAL SCIENCE BOARD DR. JOHN A. ARMSTRONG, IBM Vice President for DR. MICHAEL G. ROSSMANN, Hanley Professor of Science & Technology (retired) Biological Sciences, Purdue University DR. NINA V. FEDOROFF, Willaman Professor of Life DR. VERA RUBIN, Research Staff, Astronomy, Sciences and Director, Life Sciences Consortium and Department of Terrestrial Magnetism, Carnegie Biotechnology Institute, The Pennsylvania State Institution of Washington University DR. MAXINE SAVITZ, General Manager, Technology DR. PAMELA A. FERGUSON, Professor of Partnerships, Honeywell, Torrance, CA Mathematics, Grinnell College, Grinnell, IA DR. LUIS SEQUEIRA, J.C. Walker Professor Emeritus, DR. MARY K. GAILLARD, Professor of Physics, Theory Departments of Bacteriology and Plant Pathology, Group, Lawrence Berkeley National Laboratory University of Wisconsin, Madison DR. M.R.C. GREENWOOD, Chancellor, University of DR. DANIEL SIMBERLOFF, Nancy Gore Hunger California, Santa Cruz Professor of Environmental Science, University of Tennessee DR. STANLEY V. JASKOLSKI, Chief Technology Officer and Vice President, Technical Management, Eaton DR. BOB H. SUZUKI, President, California State Corporation, Cleveland, OH Polytechnic University, Pomona DR. ANITA K. JONES Vice Chair, Lawrence R. Quarles DR. RICHARD TAPIA, Noah Harding Professor of Professor of Engineering and Applied Science, Computational & Applied Mathematics, Rice University University of Virginia DR. CHANG-LIN TIEN, NEC Distinguished Professor DR. EAMON M. KELLY Chair, President Emeritus and of Engineering, University of California, Berkeley Professor, Payson Center for International Development & Technology Transfer, Tulane University DR. WARREN M. WASHINGTON, Senior Scientist and Section Head, National Center for Atmospheric DR. GEORGE M. LANGFORD, Professor, Department Research (NCAR) of Biological Science, Dartmouth College DR.