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Company Profiles Zhejiang Huahai Pharmaceutical Co Ltd
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Download or read book China Stock Directory written by and published by SinoMedia (Holdings) Co. Ltd.. This book was released on with total page 997 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Complete China Stock Directory written by and published by . This book was released on 2004 with total page 680 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book China Rx written by Rosemary Gibson and published by Prometheus Books. This book was released on 2018 with total page 306 pages. Available in PDF, EPUB and Kindle. Book excerpt: Millions of Americans are taking prescription drugs made in China and don't know it-- and pharmaceutical companies are not eager to tell them. This probing book examines the implications for the quality and availability of vital medicines for consumers. Several decades ago, penicillin, vitamin C, and many other prescription and over-the-counter products were manufactured in the United States. But with the rise of globalization, antibiotics, antidepressants, birth control pills, blood pressure medicines, cancer drugs, among many others are made in China and sold in the United States. China's biggest impact on the US drug supply is making essential ingredients for thousands of medicines found in American homes and used in hospital intensive care units and operating rooms. The authors convincingly argue that there are at least two major problems with this scenario. First, it is inherently risky for the United States to become dependent on any one country as a source for vital medicines, especially given the uncertainties of geopolitics. For example, if an altercation in the South China Sea causes military personnel to be wounded, doctors may rely upon medicines with essential ingredients made by the adversary. Second, lapses in safety standards and quality control in Chinese manufacturing are a risk. Citing the concerns of FDA officials and insiders within the pharmaceutical industry, the authors document incidents of illness and death caused by contaminated medications that prompted reform. This is a disturbing, well-researched book and a wake-up call for improving the current system of drug supply and manufacturing.
Book Synopsis Organic Chemistry of Drug Degradation by : Min Li
Download or read book Organic Chemistry of Drug Degradation written by Min Li and published by Royal Society of Chemistry. This book was released on 2012 with total page 311 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book examines drug degradation pathways with an emphasis on the underlying chemical mechanisms.
Book Synopsis Mergent International News Reports by :
Download or read book Mergent International News Reports written by and published by . This book was released on 2007 with total page 1584 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Report on Caffeine by : United States. Food and Drug Administration
Download or read book Report on Caffeine written by United States. Food and Drug Administration and published by . This book was released on 1980 with total page 182 pages. Available in PDF, EPUB and Kindle. Book excerpt: Abstract: Recent research on caffeine--its metabolism, teratogenic properties, and relationship to problems in pregnancy--are presented in a report to the Food and Drug Administration. Animal studies demonstrate the health implications of excessive caffeine consumption during gestation. Human epidemiologic data is extensively reviewed and found inadequate in assessing and association between caffeine exposure and fetal abnormalities. Further studies of the biologic effects of caffeine in humans are recommended.
Book Synopsis Building Shanghai by : Edward Denison
Download or read book Building Shanghai written by Edward Denison and published by Academy Press. This book was released on 2006 with total page 264 pages. Available in PDF, EPUB and Kindle. Book excerpt: Shanghai's illustrious history and phenomenal future is celebrated in this book, which examines the evolution of the city's architecture and urban form in order to contextualise the challenges facing the city today. The physical legacies that reflect Shanghai's uniqueness historically and contemporarily are examined chronologically using specific case studies of exemplary architecture interwoven in a compelling narrative that unlocks the many mysteries surrounding this amazing metropolis. Some of the most influential colonial architecture in the world, outstanding examples of Modernism and Art Deco, and an exceptional selection of eclectic and vernacular architecture reflecting Shanghai's many adopted cultures are revealed. This is the first book ever to examine this remarkable subject in a manner that is both comprehensive and captivating in its written content and stunningly illustrated with over 300 archive and contemporary photographs and maps.
Download or read book Who Owns Whom written by and published by . This book was released on 2003 with total page 1070 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Governing Health in Contemporary China by : Yanzhong Huang
Download or read book Governing Health in Contemporary China written by Yanzhong Huang and published by Routledge. This book was released on 2015-03-24 with total page 190 pages. Available in PDF, EPUB and Kindle. Book excerpt: The lack of significant improvement in people’s health status and other mounting health challenges in China raise a puzzling question about the country’s internal transition: why did the reform-induced dynamics produce an economic miracle, but fail to reproduce the success Mao had achieved in the health sector? This book examines the political and policy dynamics of health governance in post-Mao China. It explores the political-institutional roots of the public health and health care challenges and the evolution of the leaders’ policy response in contemporary China. It argues that reform-induced institutional dynamics, when interacting with Maoist health policy structure in an authoritarian setting, have not only contributed to the rising health challenges in contemporary China, but also shaped the patterns and outcomes of China’s health system transition. The study of China’s health governance will further our understanding of the evolving political system in China and the complexities of China’s rise. As the world economy and international security are increasingly vulnerable to major disease outbreaks in China, it also sheds critical light on China’s role in global health governance.
Book Synopsis Pharmaceutical Care in Digital Revolution by : Claudia Rijcken
Download or read book Pharmaceutical Care in Digital Revolution written by Claudia Rijcken and published by Academic Press. This book was released on 2019-03-15 with total page 366 pages. Available in PDF, EPUB and Kindle. Book excerpt: Pharmaceutical Care in Digital Revolution demonstrates how blending human and digital pharmaceutical care can establish optimal Apothecary Intelligence (AI). Organized into four parts, it examines digital health advances that will synergize the pharmaceutical care process and prepares stakeholders for a dynamic future, fueled with innovation. Beginning with the global picture on health care systems, patients' expectations, and current pharmaceutical care practices, the book covers details of relevant digital technologies as well as compliance, ethical, educational, and cultural aspects to take successful steps towards digital pharmaceutical care. The text includes links to lectures and technology facts, tutorials on how to implement advances in your own working environment, and examples of stakeholders who are successful in building synergy between digital and pharma. Pharmaceutical Care in Digital Revolution is a practical resource to equip pharmaceutical care stakeholders, such as pharmacists, physicians, pharmacy technicians, and students as well as those in surrounding ecosystems like payers or regulators. It is a crucial reference to understand how technological innovation is changing the paradigm in which we provide current and future pharmaceutical care and how to keep it accessible, affordable, and sustainable. - Learn about advances in digital health technology and apply them as a change leader to create circular pharmaceutical care - Provides insights on future pharmaceutical care and implement essential conditions to create the best outlook for patients - Access links, QR codes, and explanatory animations as educational material to the book
Book Synopsis Financial Report for the Fiscal Year Ended by : Cornell University
Download or read book Financial Report for the Fiscal Year Ended written by Cornell University and published by . This book was released on 1911 with total page 938 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Bottle of Lies written by Katherine Eban and published by HarperCollins. This book was released on 2020-06-23 with total page 523 pages. Available in PDF, EPUB and Kindle. Book excerpt: A NEW YORK TIMES BESTSELLER * New York Times Notable Book * Best Book of the Year: New York Public Library, Kirkus Reviews, Science Friday With a new postscript by the author From an award-winning journalist, an explosive narrative investigation of the generic drug boom that reveals fraud and life-threatening dangers on a global scale—The Jungle for pharmaceuticals Many have hailed the widespread use of generic drugs as one of the most important public-health developments of the twenty-first century. Today, almost 90 percent of our pharmaceutical market is comprised of generics, the majority of which are manufactured overseas. We have been reassured by our doctors, our pharmacists and our regulators that generic drugs are identical to their brand-name counterparts, just less expensive. But is this really true? Katherine Eban’s Bottle of Lies exposes the deceit behind generic-drug manufacturing—and the attendant risks for global health. Drawing on exclusive accounts from whistleblowers and regulators, as well as thousands of pages of confidential FDA documents, Eban reveals an industry where fraud is rampant, companies routinely falsify data, and executives circumvent almost every principle of safe manufacturing to minimize cost and maximize profit, confident in their ability to fool inspectors. Meanwhile, patients unwittingly consume medicine with unpredictable and dangerous effects. The story of generic drugs is truly global. It connects middle America to China, India, sub-Saharan Africa and Brazil, and represents the ultimate litmus test of globalization: what are the risks of moving drug manufacturing offshore, and are they worth the savings? A decade-long investigation with international sweep, high-stakes brinkmanship and big money at its core, Bottle of Lies reveals how the world’s greatest public-health innovation has become one of its most astonishing swindles.
Book Synopsis Water Pollution Control Engineering by : Great Britain. Central Office of Information
Download or read book Water Pollution Control Engineering written by Great Britain. Central Office of Information and published by . This book was released on 1970 with total page 148 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Bottles of Lies written by Katherine Eban and published by . This book was released on 2019-07 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: "Many have hailed the widespread use of generic drugs as one of the most important public-health developments of the twenty-first century. Today, almost 90 percent of our pharmaceutical market is comprised of generics, the majority of which are manufactured overseas. We have been reassured by our doctors, our pharmacists and our regulators that generic drugs are identical to their brand-name counterparts, just less expensive. But is this really true? Katherine Eban's Bottle of Lies exposes the deceit behind generic-drug manufacturing--and the attendant risks for global health. Drawing on exclusive accounts from whistleblowers and regulators, as well as thousands of pages of confidential FDA documents, Eban reveals an industry where fraud is rampant, companies routinely falsify data, and executives circumvent almost every principle of safe manufacturing to minimize cost and maximize profit, confident in their ability to fool inspectors. Meanwhile, patients unwittingly consume medicine with unpredictable and dangerous effects. The story of generic drugs is truly global. It connects middle America to China, India, sub-Saharan Africa and Brazil, and represents the ultimate litmus test of globalization: what are the risks of moving drug manufacturing offshore, and are they worth the savings?"--Dust jacket.
Author :U.s. Food and Drug Administration Publisher :Createspace Independent Pub ISBN 13 :9781500422288 Total Pages :34 pages Book Rating :4.4/5 (222 download)
Book Synopsis Avoid Food-Drug Interactions by : U.s. Food and Drug Administration
Download or read book Avoid Food-Drug Interactions written by U.s. Food and Drug Administration and published by Createspace Independent Pub. This book was released on 2014-07-05 with total page 34 pages. Available in PDF, EPUB and Kindle. Book excerpt: What you eat and drink can affect the way your medicines work. Use this guide to alert you to possible "food-drug interactions" and to help you learn what you can do to prevent them. In this guide, a food-drug interaction is a change in how a medicine works caused by food, caffeine, or alcohol. A food-drug interaction can: prevent a medicine from working the way it should cause a side effect from a medicine to get worse or better cause a new side effect A medicine can also change the way your body uses a food. Any of these changes can be harmful. This guide covers interactions between some common prescription and over-the counter medicines and food, caffeine, and alcohol. These interactions come from medicine labels that FDA has approved. This guide uses the generic names of medicines, never brand names.
Book Synopsis Exploring the Growing U.S. Reliance on China's Biotech and Pharmaceutical Products - 2019 Safety and Supply Concerns about Critical Drugs, Generics, Biologics, and Health Products, Export of Fentanyl by : Senate of the United States of America
Download or read book Exploring the Growing U.S. Reliance on China's Biotech and Pharmaceutical Products - 2019 Safety and Supply Concerns about Critical Drugs, Generics, Biologics, and Health Products, Export of Fentanyl written by Senate of the United States of America and published by . This book was released on 2019-08-11 with total page 174 pages. Available in PDF, EPUB and Kindle. Book excerpt: This report presents the hearing record of a vital Commission investigation conducted on July 31, 2019. The hearing assessed China's role in global health, pharmaceuticals, and medical products. In addition, it examined the activities of Chinese health and biotech firms in the United States, and U.S. access to China's health market. Finally, the hearing considered the implications for U.S. public health and national security of growing U.S. dependence on Chinese health products.Contents: 1. Opening Statement of Senator Talent * 2. Panel I: Administration Views on Chinese Pharmaceutical, Medical Product, and Biotechnology Development and Sourcing * 3. Christopher Priest, Chief of Staff, Defense Health Agency Operations Directorate (J-3) * 4. Panel II: China's Role in Global Health and Activities in the United States * 5. Rosemary Gibson, Senior Advisor, Hastings Center, Author, "China Rx" * 6. Ben Westhoff, Author, "Fentanyl, Inc." * 7. Dr. Jennifer Bouey, Tang Chair in China Policy Studies, RAND Corporation; Associate Professor, Georgetown University's School of Nursing and Health Studies * 8. Dr. Mark Kazmierczak, Scientist and Associate, Gryphon Scientific LLC * 9. Panel III: U.S.-China Links in Health and Medical Products: Risks and Opportunities * 10. Benjamin Shobert, Director of Strategy for Health Business Strategy, Microsoft; Senior Associate, National Bureau of Asian Research * 11. Katherine Eban, Author, "Bottle of Lies" * 12. Dr. Yanzhong Huang, Senior Fellow for Global Health, Council on Foreign Relations; Professor, School of Diplomacy and International Relations, Seton Hall University * 13. Craig Allen, President, US-China Business Council * 14. Mark Abdoo, Associate Commissioner for Global Policy and Strategy, Food and Drug AdministrationChina has emerged as the second largest pharmaceutical market in the world by revenue only behind the United States. There are several factors contributing to China's attractiveness as both a market and a production site including the low cost of production, a large consumer base, and a deep talent pool. And as China's market power continues to expand, U.S. consumers are becoming increasingly reliant on drugs sourced from the country which presents economic and national security risks. As the largest source of fentanyl, China also plays a key role in the on-going U.S. opioid epidemic. Beijing's weak regulatory and enforcement regime allows chemical and pharmaceutical manufacturers to export dangerous controlled and uncontrolled substances.What is the quality and safety of those products and what is our exposure? Should the public be concerned? Should they have more information? Are the regulatory standards sufficient to protect their interests, and how are the facilities being inspected? These are important questions, but they just touch the surface of bilateral health sector relationships between the U.S. and China.
Book Synopsis A Practical Guide to FDA's Food and Drug Law and Regulation, Seventh Edition by : Stephen M. Kanovsky
Download or read book A Practical Guide to FDA's Food and Drug Law and Regulation, Seventh Edition written by Stephen M. Kanovsky and published by . This book was released on 2020-09 with total page 672 pages. Available in PDF, EPUB and Kindle. Book excerpt: FDLI's popular reference book, A Practical Guide to FDA's Food and Drug Law and Regulation, Seventh Edition, provides an introduction to the laws and regulations governing development, marketing, and sale of FDA-regulated products, including topics on food, drugs, medical devices, biologics, dietary supplements, cosmetics, new animal drugs, cannabis, and tobacco and nicotine products. Structured to serve as a reference and as a teaching tool, the book offers practical legal and regulatory fundamentals, and each chapter builds sequentially from the last to provide an accessible overview of the key topics relevant to practitioners of food and drug law and regulation. This book is a standard legal text in law schools and graduate regulatory programs and has been cited as a reference in judicial opinions (including the U.S. Supreme Court). This Seventh Edition includes new sections on controlled substances, compounded drugs, and cannabis and cannabis-derived compounds. It also incorporates the latest amendments to the Federal Food, Drug, and Cosmetic Act, as well as FDA regulations and guidances.