124 Pages
by
CRC Press
128 Pages
by
CRC Press
Also available as eBook on:
This volume provides an introduction to the process of clinical drug development. It demystifies the way new medicines are discovered, tested and regulated. This book is intended for those who wich to understand the background of clinical trials from a pharmaceutical company perspective, and is suitable for clinical trials supplies technicians and pharmacists, data management staff, information... Read more
1: Drug Development; 2: Regulation of Drug Research; 3: Good Clinical Practice; 4: Clinical Investigators; 5: Trial Design and Protocols; 6: Case Record Forms; 7: Trial Supplies; 8: Clinical Research Associates; 9: Monitoring and Adverse Events; 10: Analysis and Reports; 11: Standard Operating Procedures (SOPs), Audits and Archives
Biography
Ann Raven, Frank Wells
