Muutke küpsiste eelistusi

Cancer Clinical Trials: Proactive Strategies Softcover reprint of the original 1st ed. 2007 [Pehme köide]

  • Formaat: Paperback / softback, 320 pages, kõrgus x laius: 235x155 mm, kaal: 522 g, XX, 320 p., 1 Paperback / softback
  • Sari: Cancer Treatment and Research 132
  • Ilmumisaeg: 22-Oct-2016
  • Kirjastus: Springer-Verlag New York Inc.
  • ISBN-10: 1489978909
  • ISBN-13: 9781489978905
Teised raamatud teemal:
  • Pehme köide
  • Hind: 141,35 €*
  • * hind on lõplik, st. muud allahindlused enam ei rakendu
  • Tavahind: 166,29 €
  • Säästad 15%
  • Raamatu kohalejõudmiseks kirjastusest kulub orienteeruvalt 2-4 nädalat
  • Kogus:
  • Lisa ostukorvi
  • Tasuta tarne
  • Tellimisaeg 2-4 nädalat
  • Lisa soovinimekirja
  • Formaat: Paperback / softback, 320 pages, kõrgus x laius: 235x155 mm, kaal: 522 g, XX, 320 p., 1 Paperback / softback
  • Sari: Cancer Treatment and Research 132
  • Ilmumisaeg: 22-Oct-2016
  • Kirjastus: Springer-Verlag New York Inc.
  • ISBN-10: 1489978909
  • ISBN-13: 9781489978905
Teised raamatud teemal:

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. The book has a foreword by Samuel A. Wells, Jr., MD, Professor of Surgery, Duke University Medical Center, Durham, NC, former Director of the American College of Surgeons and Founder of the American College of Surgeons Oncology Group.



Clinical trials are 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 a spectrum of important topics.

Historical Perspective and Evolving Concerns for Human Research.- Cancer
Trials and the Institutional Review Board (IRB).- NCIs Cancer Therapy
Evaluation Program: A Commitment to Treatment Trials.- The Role of the FDA in
Cancer Clinical Trials.- The Role of Cooperative Groups in Cancer Clinical
Trials.- The Advocate Role in Clinical Study Development and Partnering with
Patient Advocates in Your Local Institution.- The National Breast Cancer
Coalition: Setting the Standard for Advocate Collaboration in Clinical
Trials.- The Role of the Principal Investigator in Cancer Clinical Trials.-
The Audit Process and How to Ensure a Successful Audit.- The Privacy Rule
(HIPAA) as it Relates to Clinical Research.- The Commission on Cancer,
American College of Surgeons Response to HIPAA.- Ethical and Legal Issues in
the Conduct of Cancer Clinical Trials.- The Role of the Office of Research
Integrity in Cancer Clinical Trials.- Strategies for the Administration of a
Clinical Trials Infrastructure: Lessons from a Comprehensive Cancer Center.-
The Clinical Research Process: Building a System in Harmony with its Users.-
Cancer Research and Clinical Trial in Action: An Important Exercise Before
You Embark on Your Study.