Conducting GCP-compliant Clinical Research( book to Read)

The overall aim of this work is to provide a reference book which describes the general framework for conducting GCP compliant clinical research, particularly pharmaceutical industry clinical research. Hopefully, it is written in simple enough language so that it is readable to those who are new to the business: however, we have also included many examples from our years of practice to sustain the interest of a more experienced group. Pharmaceutical industry personnel (e.g. monitors, data management personnel, statisticians, medical advisers, and study medication or device suppliers from both sponsors and CROs) will find many helpful hints and examples of how the situation can go awry.