This easy-to-read reference book provides a practical approach for dealing with the legal and regulatory compliance issues involved in human research. Covering

Regulatory bodies such as the European Medicine Agency have done tremendous work in collaboration with experts from the field to develop Good Clinical Practices

Data sharing can accelerate new discoveries by avoiding duplicative trials, stimulating new ideas for research, and enabling the maximal scientific knowledge an

The second edition of this innovative work again provides a unique perspective on the clinical discovery process by providing input from experts within the NIH

Successful drug development relies on accurate and efficient clinical trials to deliver the best and most effective pharmaceuticals and clinical care to patient