Optimizing Clinical Trials: A Comprehensive Guide for Researchers and Clinicians

Clinical trials have revolutionized the treatment of diseases and the development of life-saving pharmaceuticals. They play a crucial role in diagnosis, prevention of early death, medical intervention, and are central to the modern work of pharmaceutical producers. The design and execution of clinical trials is one of the fastest-growing and most important areas of medical and pharmaceutical research.

A Concise Guide to Clinical Trials: Your Trusted Resource

A Concise Guide to Clinical Trials provides an accessible and comprehensive survey of clinical trials, their design, and their applications. This updated resource begins with a taxonomy of trial types, overviews stages of analysis, ethical and legal requirements, and more. With its easy-to-use organization, it facilitates both first-time learning and reference.

Stay up-to-date with the latest research and clinical practice with new material on:

• Pharmaceutical trials and their importance in the industry
• Adaptive designs and their applications in clinical research
• The role of big data in clinical trials and its potential benefits

In addition, this guide covers crucial concepts such as:

• Health technology assessments (HTA) and their impact on clinical practice
• Patient and public involvement and engagement (PPIE) in clinical trials
• And more

Ideal for clinicians and healthcare professionals looking for a working knowledge of clinical trials, A Concise Guide to Clinical Trials is also an invaluable resource for pharmaceutical workers and regulators looking to understand this vital aspect of the industry.

Publisher: Wiley
Publication Date: May 7, 2024
Language: English
ISBN: 9781119502807, 9781119502777