Clinical Trials Comprehending the Future
This book is of 'a must read' category, and a quality reference for professionals associated directly or indirectly to the world of pharma Clinical Trials. It is aimed to assist the companies which are trying to manage clinical trials efficiently, planning to improve clinical trials, struggling to handle outsourced clinical trials and integration of clinical trials. It is a good choice for anyone who thinks of ethics in clinical trials, Improved Pharmaceutical clinical trials, research and development of pharma products, and shortening the development timelines -which can play a vital role in achieving the company's goals.
The book is also supportive to carry out cost-effective clinical research, preclinical research, clinical trial integration, clinical and non-clinical investigations, and retention of subjects for clinical research. It further provides information regarding innovative approaches, trends and supply chain of clinical trials, along with some insights into clinical trials outsourcing- Asian opportunities & competitive advantage.
- Off shoring -- Cost-effective clinical research
- Ethics in Clinical Trials and Drug Development
- Unleashing the Industry's True Potential Closed loop clinical trial supply chain
- Improving Pharmaceutical R&D Using Lean Sigma
- Preclinical Research in Big Biotech Vertical integration is the key
- Early Formulation Shortening the development timelines
- Clinical and Non-Clinical Investigations Improving the quality of development candidates
- Clinical Trial Integration - Adopting an innovative approach
- Foreign Biotech Trials in Asia Emerging trends
- Site Management Organisations in Asian Clinical Trials Providing competitive advantage
- Asian Clinical Trials Managing patient reported outcomes
- Clinical Trials in China & Japan Dynamic opportunities for sponsors and CROs
- Retention of Subjects The question of informed consent
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