Cancer clinical trials : proactive strategies /
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Imprint: | New York : Springer, c2007. |
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Description: | xv, 318 p. : ill. ; 25 cm. |
Language: | English |
Series: | Cancer treatment and research ; 132 Cancer treatment and research ; v. 132. |
Subject: | |
Format: | Print Book |
URL for this record: | http://pi.lib.uchicago.edu/1001/cat/bib/6234976 |
Table of Contents:
- Contributors
- Foreword
- Preface
- Acknowledgement
- 1. Historical Perspective and Evolving Concerns for Human Research
- 2. Cancer Trials and the Institutional Review Board (IRB)
- 3. NCI's Cancer Therapy Evaluation Program: A Commitment to Treatment Trials
- 4. Practical Guide for Cancer Clinical Investigators
- 5. The Role of Cooperative Groups in Cancer Clinical Trials
- 6. The Advocate Role in Clinical Study Development and Partnering with Patient Advocates in Your Local Institution
- 7. The National Breast Cancer Coalition: Setting the Standard for Advocate Collaboration in Clinical Trials
- 8. The Role of the Principal Investigator in Cancer Clinical Trials
- 9. The Audit Process and How to Ensure a Successful Audit
- 10. The Privacy Rule (HIPAA) As It Relates To Clinical Research
- 11. The Commission on Cancer, American College of Surgeons' Response to HIPAA
- 12. Ethical and Legal Issues in the Conduct of Cancer Clinical Trials
- 13. The Role of the Office of Research Integrity in Cancer Clinical Trials
- 14. Strategies for the Administration of a Clinical Trial Infrastructure: Lessons from a Comprehensive Cancer Center
- 15. The Clinical Research Process: Building a System in Harmony with Its Users
- 16. Cancer Research and Clinical Trial in Action: An Important Exercise Before You Embark on Your Study
- Index