Download or read book Case Studies of Regulatory Acceptance written by Interstate Technology and Regulatory Cooperation Work Group and published by . This book was released on 1996 with total page 62 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Case Studies on the Regulatory Challenges Raised by Innovation and the Regulatory Responses written by OECD and published by OECD Publishing. This book was released on 2021-12-14 with total page 150 pages. Available in PDF, EPUB and Kindle. Book excerpt: The pace and scope of innovation are challenging the way governments regulate. Existing regulatory frameworks might not be agile enough to accommodate the fast pace of technological development and, as a consequence, rules might become outdated.
Download or read book Regulatory Breakdown written by Cary Coglianese and published by University of Pennsylvania Press. This book was released on 2012-08-16 with total page 290 pages. Available in PDF, EPUB and Kindle. Book excerpt: Regulatory Breakdown: The Crisis of Confidence in U.S. Regulation brings fresh insight and analytic rigor to what has become one of the most contested domains of American domestic politics. Critics from the left blame lax regulation for the housing meltdown and financial crisis—not to mention major public health disasters ranging from the Gulf Coast oil spill to the Upper Big Branch Mine explosion. At the same time, critics on the right disparage an excessively strict and costly regulatory system for hampering economic recovery. With such polarized accounts of regulation and its performance, the nation needs now more than ever the kind of dispassionate, rigorous scholarship found in this book. With chapters written by some of the nation's foremost economists, political scientists, and legal scholars, Regulatory Breakdown brings clarity to the heated debate over regulation by dissecting the disparate causes of the current crisis as well as analyzing promising solutions to what ails the U.S. regulatory system. This volume shows policymakers, researchers, and the public why they need to question conventional wisdom about regulation—whether from the left or the right—and demonstrates the value of undertaking systematic analysis before adopting policy reforms in the wake of disaster.
Download or read book International Regulatory Co operation written by Organisation for Economic Co-Operation and Development (OECD) and published by IWA Publishing. This book was released on 2013-06-06 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: The world is becoming increasingly global. This raises important challenges for regulatory processes which still largely emanate from domestic jurisdictions. In order to eliminate unnecessary regulatory divergences and to address the global challenges pertaining to systemic risks, the environment, and human health and safety, governments increasingly seek to better articulate regulations across borders and to ensure greater enforcement of rules. But, surprisingly, the gains that can be achieved through greater co-ordination of rules and their application across jurisdictions remain largely under-analysed. This volume complements the stocktaking report on International Regulatory Co-operation: Rules for a Global World by providing evidence on regulatory co-operation in the area of transboundary water management and through the fast development of transnational private regulation.
Download or read book Strengthening a Workforce for Innovative Regulatory Science in Therapeutics Development written by Institute of Medicine and published by National Academies Press. This book was released on 2012-04-04 with total page 118 pages. Available in PDF, EPUB and Kindle. Book excerpt: The development and application of regulatory science - which FDA has defined as the science of developing new tools, standards, and approaches to assess the safety, efficacy, quality, and performance of FDA-regulated products - calls for a well-trained, scientifically engaged, and motivated workforce. FDA faces challenges in retaining regulatory scientists and providing them with opportunities for professional development. In the private sector, advancement of innovative regulatory science in drug development has not always been clearly defined, well coordinated, or connected to the needs of the agency. As a follow-up to a 2010 workshop, the IOM held a workshop on September 20-21, 2011, to provide a format for establishing a specific agenda to implement the vision and principles relating to a regulatory science workforce and disciplinary infrastructure as discussed in the 2010 workshop.
Download or read book International Regulatory Co operation Case Studies Vol 1 Chemicals Consumer Products Tax and Competition written by OECD and published by OECD Publishing. This book was released on 2013-05-31 with total page 88 pages. Available in PDF, EPUB and Kindle. Book excerpt: This volume complements the stocktaking report on International Regulatory Co-operation: Rules for a Global World by providing evidence on regulatory co-operation in four sectors: chemical safety, consumer product safety, model tax convention, and competition law enforcement.
Download or read book The Governance of Effective Regulatory Co operation written by G. Bruce Doern and published by . This book was released on 2004 with total page 46 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book The Political Economy of Local Regulation written by Alberto Asquer and published by Springer. This book was released on 2016-10-26 with total page 389 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book offers theoretical and methodological guidelines for researching the complex regulation of local infrastructure, utilities and public services in the context of rapid urbanisation, technological change, and climate change. It examines the interactions between regulators, public officers, infrastructure and utilities firms, public service providers, citizens, and civil society organisations. It contains contributions from academics and practitioners from various disciplinary perspectives and from many regions of the world, illustrated with case studies from several sectors including water, natural gas and electricity distribution, local public transport, district heating, urban waste, and environmental services.
Download or read book The Changing Economics of Medical Technology written by Institute of Medicine and published by National Academies Press. This book was released on 1991-02-01 with total page 225 pages. Available in PDF, EPUB and Kindle. Book excerpt: Americans praise medical technology for saving lives and improving health. Yet, new technology is often cited as a key factor in skyrocketing medical costs. This volume, second in the Medical Innovation at the Crossroads series, examines how economic incentives for innovation are changing and what that means for the future of health care. Up-to-date with a wide variety of examples and case studies, this book explores how payment, patent, and regulatory policiesâ€"as well as the involvement of numerous government agenciesâ€"affect the introduction and use of new pharmaceuticals, medical devices, and surgical procedures. The volume also includes detailed comparisons of policies and patterns of technological innovation in Western Europe and Japan. This fact-filled and practical book will be of interest to economists, policymakers, health administrators, health care practitioners, and the concerned public.
Download or read book Impact of Regulatory Compliance Costs on Small Airports written by and published by . This book was released on 2013 with total page 96 pages. Available in PDF, EPUB and Kindle. Book excerpt: "TRB's Airport Cooperative Research Program (ACRP) Report 90: Impact of Regulatory Compliance Costs on Small Airports explores the cumulative costs of complying with regulatory and other federal requirements at small hub and non-hub airports."--Publisher's description.
Download or read book Regulatory Policy and Behavioural Economics written by Lunn Pete and published by OECD Publishing. This book was released on 2014-01-10 with total page 74 pages. Available in PDF, EPUB and Kindle. Book excerpt: This study offers an international review of the initial applications of behavioural economics to policy, with a particular focus on regulatory policy.
Download or read book International Regulatory Co operation Case Studies Vol 2 Canada US Co operation EU Energy Regulation Risk Assessment and Banking Supervision written by OECD and published by OECD Publishing. This book was released on 2013-06-05 with total page 88 pages. Available in PDF, EPUB and Kindle. Book excerpt: This volume complements the stocktaking report on International Regulatory Co-operation: Rules for a Global World by providing evidence on regulatory co-operation in the Canada-U.S. Regulatory Cooperation Council, as part of EU energy regulation, under the Global Risk Assessment Dialogue, etc.
Download or read book Preventing Regulatory Capture written by Daniel Carpenter and published by Cambridge University Press. This book was released on 2014 with total page 531 pages. Available in PDF, EPUB and Kindle. Book excerpt: Leading scholars from across the social sciences present empirical evidence that the obstacle of regulatory capture is more surmountable than previously thought.
Download or read book Case Studies on the Regulatory Challenges Raised by Innovation and the Regulatory Responses written by Oecd and published by Org. for Economic Cooperation & Development. This book was released on 2021-12-23 with total page 148 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Recommendation of the Council on Regulatory Policy and Governance written by OECD and published by OECD Publishing. This book was released on 2012-11-02 with total page 38 pages. Available in PDF, EPUB and Kindle. Book excerpt: This set of guidelines provides the measures by which governments can implement or advance regulatory reform.
Download or read book What Went Wrong Pharma Tech Case Studies Pharma Regulatory Investigations written by and published by Notion Press. This book was released on 2020-06-11 with total page 158 pages. Available in PDF, EPUB and Kindle. Book excerpt: The objective of What Went Wrong? Pharma Tech Case Studies is to provide multidisciplinary approaches/guidelines for problem-solving capability. These case studies are based on the actual situation faced by the author in India and overseas and successfully resolved with the back-up of science and technology convincing international regulators/complainants leading to the closing of complaints. The book provides guidelines covering regulatory requirements for documentation. How do you document (format) any complaint? How to investigate a case study, using knowledge of science and technology and method of investigation? How to reproduce the complaint in-house, where ever required? It answers these various questions. The conclusion is with corrective and preventive actions required, submission of the investigation report and assignable reason to the regulatory agency/complainant, getting a response from the complainant and once satisfied, requesting them to close the complaint. Can we integrate regulatory science with other subjects of pharmaceutical sciences to learn 'What Went Wrong? In Pharma Tech Case Study'. Important regulatory references are provided at the end.
Download or read book Clinical Evaluation of Medical Devices written by Karen M. Becker and published by Humana. This book was released on 2010-11-05 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: The original edition of this text, Clinical Evaluation of Medical Devices: Principles and Case Studies, provided the first overview of key pr- ciples and approaches to medical device clinical trials, illustrated with a series of detailed, real-world case studies. The book is designed as a resource for clinical professionals and regulatory specialists working in the field of new medical device development and marketing. Since the first edition of this text was published in 1997, the rapid pace of inno- tion in health care technologies continues to yield exciting and important new products. The regulatory landscape has also evolved, reflecting some of the changes and needs within the medical device industry. The purpose of Clinical Evaluation of Medical Devices: Principles and Case Studies, Second Edition is to provide an updated and expanded presentation of the scientific methods and regulatory requirements applied to the study of new significant risk medical devices. The text now includes (1) new information on the requirements and process for gaining reimbursement of new products from Medicare and private insurers, with case studies of research specifically designed for this p- pose as well as health care technology assessment methods; (2) infor- tion on new statistical methodologies applied to medical device trials; and (3) all new case studies, including examples of combination pr- ucts, three-phase development models (i. e. , feasibility, FDA approval, Medicare reimbursement), and novel study designs.
