Delhi, India (PressExposure) July 20, 2009 -- The book provides a step by step guide for developing a clinical trial site for conducting world-class clinical trials with inbuilt tips on every aspect of the development process.
The book is aimed at providing a comprehensive understanding of new drug discovery and development process along with guidance on how to get involved in a clinical trial; constitution of study team at a site; infrastructure development; study initiation, conduct and closeout; safety reporting; informed consent process; investigational product accountability and management; maintenance of source document; completion of case report forms; HIPAA privacy rules; clinical trial monitoring; regulatory inspections etc.
âOur idea to publish the book on this topic is backed by an urge to address the unmet needs of clinicians who wants to become successful clinical trial investigatorsâ, says Mukul Singhal, Director of DNA Press.
The author of the book Dr. P. K. Julka is a well known cancer specialist of India. With over three decades of cancer treatment and research and a variety of major breakthroughs to his credit, he has treated cancer patients from all the segments of the society.
Stretching across 147 pages the book contains 26 chapters and 3 appendices that would be of great benefit to the existing as well as new investigators. The publishers can be reached at email@example.com