How to Monitor and Write Clinical Trial Monitoring Reports After Each Trial Visit in Clinical Trial Site Volume 1: This book teaches you all you need to know about how to Monitor and write a detailed Clinical trial monitoring report. The book is packed with interesting topics on how to monitor and write clinical trial monitoring reports after each site clinical visit. This book is a theoretical and practical guide on monitoring and writing clinical trial monitoring reports with samples of clinical monitoring reports in each practice exercise. This book is a masterpiece that will help you learn clinical trial monitoring and how to write a clinical trial monitoring report. It comes in as a practical workbook for clinical research associates and those aspiring to enter into clinical research, The book was written with detailed 2024 regulatory laws and ICH Good Clinical Practice Guidelines 2024/ethics, hence it is highly recommended for the above-mentioned clinical research professionals because of the above mentioned 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 monitoring and how to write a clinical trial monitoring report with scenario simulation live practical examples that will make you feel like you are in a clinical trial site with several sample examples of clinical trial monitoring reports which will enable you to learn how to monitor and write your monitoring report with ease. The contents of this book will refresh your mind about your work as Clinical Research Associate and all the monitoring methodologies, clinical trial reports, regulatory laws, and ethics /compliance with deep practical scenario live examples that will remind you of all you have learned in the past. 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 USFDA guidelines, ethical rules, and Regulatory Laws 2024 in clinical research applications, clinical trial setup, recruitment of study participants, signing of consent forms and newest GCP guidelines for 2024 and other ethical guidelines that can help you monitor your clinical trials and write a well-detailed monitoring report. . This is a must-read book that covers everything you need to know about clinical research monitoring and how you can write a clinical monitoring report with life samples of clinical trial reports that will enable you to monitor and write your monitoring report. I strongly suggest that you buy this book because I know it will be useful to you especially if you are in this profession or aspiring to become a clinical research associate. Some of the topics covered in this book are as follows, Clinical trial monitoring and what it entails. How to monitor a clinical trial How to write a clinical trial monitoring report with sample examples Four Phases of Clinical Trials. Practical scenario examples on how to monitor and write clinical trial monitoring reports. CRAs and types of monitoring visits. Practical Scenarios on protocol deviation. Practical scenario questions and answers on-site monitoring visits Clinical trial monitoring report and how to write a detailed monitoring report. Clinical trial preparation ICH-E6 Good Clinical Practice / Regulatory Guidelines 2024 Ethics in clinical research Regulatory affairs in clinical research Clinical Research Design, Protocol Design, CRF Design, and Recruitment Process . . Read more Report an issue with this product or seller ISBN-13 979-8860704343 Publication date September 8, 2023 Language English Dimensions 6 x 0.33 x 9 inches
