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Research - A Concise Guide to Clinical Trials

Description

Book Synopsis: Biopharmaceutical drugs improve the health and well-being of people across the globe on a scale that is unrivaled by any other medical intervention. Before these drugs can be prescribed for patients by their doctors, they have to be approved for marketing by a regulatory agency. To gain marketing approval, drugs must go through an extremely rigorous process that investigates their safety and efficacy, the process of New Drug Development. The last stage of this long, complex, and expensive process involves conducting clinical trials, the topic of this book. Successfully conducting clinical trials requires the interdisciplinary collaboration of individuals from many clinical and scientific disciplines and areas of operational expertise. These include medicine, information technology, ethics and law, statistics, clinical trial operations, data collection and management, regulatory science, and medical writing, to name just a few. Central aspects of conducting clinical trials are discussed in the following chapters, with the goals of making specialists from each of these areas aware of the contributions of their colleagues, and helping readers to appreciate that everyone involved in clinical research is working side-by-side toward a common goal---improving the health, well-being, and longevity of millions of patients around the globe.

Details

Looking to improve healthcare on a global scale? Introducing our groundbreaking book, "A Concise Guide to Clinical Trials" - the ultimate resource for understanding the rigorous process of drug development and the vital role of clinical trials in bringing life-changing medications to patients. With a strong emphasis on safety and efficacy, this comprehensive guide provides valuable insights into the interdisciplinary collaboration required to successfully conduct clinical trials. From medicine to statistics, ethics to regulatory science, this book covers it all. Join us in the journey of improving the health, well-being, and longevity of millions of patients worldwide.

Unlock the secrets of the pharmaceutical world and gain a profound understanding of the critical stages leading up to the marketing approval of biopharmaceutical drugs. "A Concise Guide to Clinical Trials" takes you on an enlightening journey through the complex process of drug development. Learn how dedicated professionals from diverse backgrounds and areas of expertise come together to ensure every drug meets the stringent requirements for safety and efficacy. By delving into the intricacies of clinical trial operations, data management, and medical writing, this book offers a complete picture of the collaborative effort behind groundbreaking medical advancements.

Our team of renowned experts has meticulously compiled all the essential information you need to comprehend the extensive world of clinical trials. Dive into the chapters of this invaluable resource and witness the amazing work done by statisticians, physicians, regulatory specialists, and countless others who dedicate their lives to improving global healthcare. Through the lens of this book, you'll gain a deep appreciation for the tireless efforts of everyone involved in clinical research, all striving toward a common goal - improving the lives of patients worldwide.

Ready to join the ranks of visionary individuals transforming the healthcare landscape? Don't miss out on the opportunity to delve into the world of clinical trials with "A Concise Guide to Clinical Trials". Explore the interconnectedness of various fields, discover the challenges faced during drug development, and realize the pivotal role clinical trials play in making medical breakthroughs possible. Click here to get your hands on this indispensable resource and become a part of the global mission to enhance the health and well-being of every patient.

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