Research is an integral component of all medical disciplines. This multi -authored book is organized into 23 chapters covering topics related to design of clinical trial, regulations governing such trials, financial management, data handling, ethics and good clinical practice. An exhaustive glossary is the asset of this book; the definitions are well written and easy to understand. The book has focus on drug trials, and covers the topics of drug development process and documentation quite well. A table or box outlining requirements under Schedule Y of Drugs and Cosmetic Rules would have enhanced the utility of the chapter on regulatory aspects. The chapter on ‘Design of Clinical Trial’ is written in simple language but lacks examples. Presenting information with examples is needed at other places too.

For a multi-authored book, some amount of duplication is expected. Information about phases of clinical trials and ethical aspects, including informed consent, is presented in many chapters by different authors. The chapter on ‘Globalization of clinical research’ is written twice (by different authors with a slight change in name). Fortunately, there is not much contradiction of information at different places. I recommend this book for clinical researchers, young research scientists, and students enrolled under clinical research training courses.

Dheeraj Shah