Clinical Research Law and Ethics Volume 2: Human Research and a Complete Theoretical and Practical Guide to Regulatory Compliance Clinical Research and Law Ethics Volume 2: 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 2 is the latest edition of the first book published earlier on and it comes with three more new topics on managing the review process, the medico documents and personality development. The book is detailed with interesting topics in clinical research, law, and ethics and a complete practical guide for human research, and a detailed monitoring and practical guide in clinical trial research from scratch to finish with great emphasis on life practical scenarios and illustrations. 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 on training, 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 and the preparation, research design, protocol design, case report form designs, biostatistics/data management from scratch to finish. This book will refresh your mind about your work in clinical research and all regulatory laws and ethics /compliance with deep practical scenario life examples that will remind all you have learned in the past, with new things added in the book like medical writing that will interest you the more. It is written with a complete theoretical and practical guide for clinical research associates and it will teach you all you need to know about the current FDA guidelines, ethical rules, and concepts in clinical research applications, clinical trial setup, recruitment of study participants, signing of consent forms and newest GCP guidelines for 2023 and other ethical guidelines that can help you monitor your clinical trials effectively. . 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 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 Practical Section Scenario practical Questions and Answers. Managing the review process Medico documents Read more Report an issue with this product or seller ISBN-13 979-8850205065 Publication date June 28, 2023 Language English Dimensions 6 x 0.8 x 9 inches Next slide of product details See all details
