Original PDF Ebook – The Sourcebook for Clinical ResearchA Practical Guide for Study Conduct – 9780128162422

Original PDF Ebook – The Sourcebook for Clinical ResearchA Practical Guide for Study Conduct – 9780128162422

A single trial is complex, with numerous regulations, administrative processes, medical procedures, deadlines and specific protocol instructions to follow. And yet, there has existed no single-volume, comprehensive clinical research reference manual for investigators, medical institutions, and national and international research personnel to keep on the shelf as a ready reference to navigate through trial complexities and ensure compliance with U.S. Federal Regulations and ICH GCP until The Sourcebook for Clinical Research. An actionable, step-by-step guide through beginning to advanced topics in clinical research with forms, templates and checklists to download from a companion website, so that study teams will be compliant and will find all the necessary tools within this book. Additionally, the authors developed Display Posters for Adverse Events Plus Reporting and Medicare Coverage Analysis that can be purchased separately here: https://www.elsevier.com/books-and-journals/book-companion/9780128162422/order-display-posters. Moreover, The Sourcebook for Clinical Research contains clear information and guidance on the newest changes in the industry to keep seasoned investigators and staff current and compliant, in addition to providing detailed information regarding the most complex topics._x000D_
This book serves as a quick, actionable, off-the-shelf resource to keep by your side at the medical clinic._x000D_
Makes vital trial conduct information easy to understand and instructs on how to practically apply current Federal regulations and Good Clinical Practice (ICH GCP)_x000D_
Offers extensive guidance that is crucial for guaranteeing compliance to clinical research regulations during each step of the clinical research process_x000D_
Provides up-to-date and extensive coverage of beginning to advanced topics, and, step-by-step actions to take during exceptional circumstances, including compassionate use, emergency use, human subjects protections for vulnerable populations, and federal audits_x000D_
Furnishes a detailed clinical research Glossary, and a comprehensive Appendix containing ready-to-use forms, templates, and checklists for clinical trial personnel to download and begin using immediately._x000D_
Written for the fast-paced clinic environment with action steps and forms in the book to respond to a research subject’s needs urgently and compliantly