Click on the link below if you want to buy this book, https://www.amazon.com/s?k=timothy+ekwebelem&ref=nb_sb_noss Clinical Research and Law Ethics Volume 3: Human Research and a Complete Practical Guide to Regulatory Compliance: This book teaches you all you need to know about clinical research and its practical guide. Clinical Research Law and Ethics Volume 3 is the latest edition of the first and second volumes published earlier, and it comes with five more new topics on managing the review process, medico documents, pharmaceutical medicine, and personality development. The book is detailed with interesting topics in clinical research, law, and ethics and a complete practical guide for human research. Clinical Research Law and Ethics Volume 3 contains extensive and detailed monitoring and a practical guide on how to run and monitor clinical trial research from scratch to finish with great emphasis on live practical scenarios, illustrations, and simulations. This book is second to none and it was written bearing in mind what happens at the clinical trial site, what a clinical research associate should know, and how he or she can successfully carry out his monitoring activities which include site selection visits, initiation visits, closeout visit and all the regulatory and international/local ethical guidelines that can help a clinical research associate to monitor his or her site activities successfully according to the ICH Good Clinical Practice. This book is a masterpiece that comes in as a practical and theoretical workbook with detailed regulatory laws and ethics for clinical research associates, principal investigators, sub-investigators, clinical trial coordinators, clinical trial physicians, medical doctors in clinical trials, medical students, clinical trial students and inhouse clinical trial associates, pharmacist, clinical trial assistance and those aspiring to go into clinical research. The book was written with detailed regulatory laws and ethical concepts, hence it is highly recommended for the above-mentioned clinical research professionals because of the important topics covered in the book. I can assure you that this is the right book for you as each chapter is packed with full captivating topics that will blow your mind and advance your knowledge in everything you need to know about clinical trial research laws and ethics/ compliance, preparation, research design, protocol design, case report form designs, biostatistics/data management from scratch to finish. This is a must-read book that covers everything you need to know about clinical research laws and ethics and the conduct of clinical research from scratch to finish. I strongly suggest that you buy this book because I know it will be useful to you and I recommend that you buy a copy for yourself, friends and work colleagues. In this book, you are also going to learn the following, Pharmaceutical Companies, CROs, and Academic sponsors Clinical Research Design, Protocol Design, CRF Design, and Recruitment Process. Four Phases of Clinical Research Clinical Trial Preparation, Study Design, and Study Start-Up. Essential Documents and Common Technical Documents Clinical Research Laws/Ethics in Clinical Research Roles and Responsibilities of Clinical Research Personnel Compliance and Audit in Clinical Research How to write Clinical Trial Monitoring Report. Therapeutic Areas in Clinical Research Data Management and Biostatistics. Basics of Medical Writing Scenario Practical Section Scenario practical Questions and Answers. Managing the review process Medico documents Personality Development Pharmaceutical medicine. Read more Report an issue with this product or seller ISBN-13 979-8342085373 Publication date October 8, 2024 Language English Dimensions 6 x 0.84 x 9 inches Next slide of product details See all details
