Intelligent Drug Development

Clinical research is heavily regulated and involves coordination of numerous pharmaceutical-related disciplines. Each individual trial involves contractual regulatory and ethics approval at each site and in each country. Clinical trials have become so complex and government requirements so stringent that researchers often approach trials too cautiously convinced that the process is bound to be insurmountably complicated and riddled with roadblocks. A step back is needed an objective examination of the drug development process as a whole and recommendations made for streamlining the process at all stages.With Intelligent Drug Development Michael Tansey systematically addresses the key elements that affect the quality timeliness and cost-effectiveness of the drug-development process and identifies steps that can be adjusted and made more efficient. Tansey uses his own experiences conducting clinical trials to create a guide that provides flexible adaptable ways of implementing the necessary processes of development. Moreover the processes described in the book are not dependent either on a particular company structure or on any specific technology; thus Tansey''s approach can be implemented at any company regardless of size. The book includes specific examples that illustrate some of the ways in which the principles can be applied as well as suggestions for providing a better context in which the changes can be implemented. The protocols for drug development and clinical research have grown increasingly complex in recent years making Intelligent Drug Development a needed examination of the pharmaceutical process.