Cancer Clinical Trials: Proactive StrategiesStanley P. L. Leong Springer Science & Business Media, 2007/11/25 - 320 ページ Clinical trials remain the most important vehicle for improving the care of cancer patients. This text presents the fundamental components and challenges involving clinical investigations. Leading experts discuss the critical issues covering the spectrum of important topics from planning to application. |
目次
Cancer Trials and the Institutional Review Board IRB | 11 |
Practical Guide for Cancer Clinical Investigators | 51 |
The Role of Cooperative Groups in Cancer Clinical | 111 |
The Advocate Role in Clinical Study Development and 131 | 130 |
The Role of the Principal Investigator in Cancer | 157 |
vi | 178 |
The Privacy Rule HIPAA As It Relates To Clinical | 199 |
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academic activities addition Administration adverse advocates agents animal application approval assessment associated assurance audit benefit biological Board breast cancer cancer clinical trials Center clinical research committee complete compliance conduct considered cooperative group described determine disease document drug educational effective enrolled ensure established ethical evaluation expected experience federal findings Food funding hold human subjects identified important improve individual industry informed consent infrastructure initial institutions Integrity interest investigators involved issues major meeting misconduct monitoring Office Oncology participation patients performance phase physician policies potential practice prevention procedures proposed protection protocol questions records regulations regulatory requirements response risk Rule safety scientific specific sponsor standards submitted therapy treatment
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