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Author: Geraint G. Howells
Publisher: Manchester University Press
Published: 1991
Total Pages: 240
ISBN-13: 9780719033742
DOWNLOAD EBOOK →A collection of papers from the ninth Fulbright Colloquium held in September 1989. The papers compare legal practices and procedures in North America and Europe and the barriers to drug development caused by increased litigation in cases involving pharmaceutical products.
Author: Steven Garber
Publisher: Rand Corporation
Published: 2013
Total Pages: 117
ISBN-13: 0833079913
DOWNLOAD EBOOK →Liability effects on the economic performance of the pharmaceutical industry play a prominent role in the debate about the economic effects of product liability in the United States. The author analyzes incentive effects on company decisions, implications for economic outcomes such as drug safety and effectiveness, and suggests how public policy changes could mitigate liability-based sources of inefficient decisions of pharmaceutical companies.
Author: Steven Garber
Publisher: RAND Corporation
Published: 1993
Total Pages: 272
ISBN-13:
DOWNLOAD EBOOK →This study examined the economic effects of product liability on firms producing drugs and medical devices. The study found that the liability system enhances the economic contributions of the industries in some ways.
Author: Institute of Medicine
Publisher: National Academies Press
Published: 1988-01-01
Total Pages: 203
ISBN-13: 0309038472
DOWNLOAD EBOOK →In the past 50 years the development of a wide range of medical devices has improved the quality of people's lives and revolutionized the prevention and treatment of disease, but it also has contributed to the high cost of health care. Issues that shape the invention of new medical devices and affect their introduction and use are explored in this volume. The authors examine the role of federal support, the decision-making process behind private funding, the need for reforms in regulation and product liability, the effects of the medical payment system, and other critical topics relevant to the development of new devices.
Author: National Research Council and Institute of Medicine
Publisher: National Academies Press
Published: 1990-01-01
Total Pages: 206
ISBN-13: 0309041473
DOWNLOAD EBOOK →There are numerous reasons to hasten the introduction of new and improved contraceptivesâ€"from health concerns about the pill to the continuing medical liability crisis. Yet, U.S. organizations are far from taking a leadership position in funding, researching, and introducing new contraceptivesâ€"in fact, the United States lags behind Europe and even some developing countries in this field. Why is research and development of contraceptives stagnating? What must the nation do to energize this critical arena? This book presents an overall examination of contraceptive development in the United Statesâ€"covering research, funding, regulation, product liability, and the effect of public opinion. The distinguished authoring committee presents a blueprint for substantial change, with specific policy recommendations that promise to gain the attention of specialists, the media, and the American public. The highly readable and well-organized volume will quickly become basic reading for legislators, government agencies, the pharmaceutical industry, private organizations, legal professionals, and researchersâ€"everyone concerned about family planning, reproductive health, and the impact of the liability and regulatory systems on scientific innovations.
