標(biāo)題: Titlebook: Cancer Clinical Trials: Proactive Strategies; Stanley P. L. Leong Book 2007 Springer-Verlag US 2007 breast cancer.cancer.cancer research.c [打印本頁] 作者: Opulent 時間: 2025-3-21 19:31
書目名稱Cancer Clinical Trials: Proactive Strategies影響因子(影響力)
作者: 憤憤不平 時間: 2025-3-21 21:47
Cancer Treatment and Researchhttp://image.papertrans.cn/c/image/221081.jpg作者: 浪蕩子 時間: 2025-3-22 01:19
Miscellaneous Issues Related to NeurotraumaIn summary, cancer clinical trials are not easy to run. Every PI should be well prepared to meet the complex challenges inherent in conducting clinical trials and be proud to be engaged in the search for a “cure” for cancer patients.作者: CAB 時間: 2025-3-22 08:36
The Role of the Principal Investigator in Cancer Clinical Trials,In summary, cancer clinical trials are not easy to run. Every PI should be well prepared to meet the complex challenges inherent in conducting clinical trials and be proud to be engaged in the search for a “cure” for cancer patients.作者: 猛烈責(zé)罵 時間: 2025-3-22 08:50
Cancer Clinical Trials: Proactive Strategies978-0-387-33225-3Series ISSN 0927-3042 Series E-ISSN 2509-8497 作者: Bumble 時間: 2025-3-22 14:24 作者: Bumble 時間: 2025-3-22 19:47
Book 2007.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..作者: 刪減 時間: 2025-3-23 00:19 作者: Femish 時間: 2025-3-23 04:56 作者: 持續(xù) 時間: 2025-3-23 07:09 作者: Canary 時間: 2025-3-23 10:07 作者: patriot 時間: 2025-3-23 14:50 作者: multiply 時間: 2025-3-23 18:18
Management of Spinal Neurotraumaany and the claims of some, the Privacy Rule need not stifle such research. By understanding all of the regulations that govern research with human subjects, including the Common Rule, FDA regulations and the Privacy Rule, investigators are able to perform scientifically sound and ethical research. 作者: 攀登 時間: 2025-3-23 23:17
Complications, Outcome, and Other Aspectsch of the programs and the ACoS. Worrisome unintended consequences, potentially threatening the value of the products that the CoC provides cancer patients, providers, and families, were not realized because of the Business Associate role that the CoC assumes with each of the CoC-Approved programs.作者: lethargy 時間: 2025-3-24 03:59
Initial Evaluation and Managementgulatory compliance environment. It is important that they avail themselves and their staff of all opportunities for education, training and professional development in the courses focused on the ethical and responsible conduct of research involving human participants. Particular attention should be作者: upstart 時間: 2025-3-24 08:54
,The Commission on Cancer, American College of Surgeons’ Response to HIPAA,ch of the programs and the ACoS. Worrisome unintended consequences, potentially threatening the value of the products that the CoC provides cancer patients, providers, and families, were not realized because of the Business Associate role that the CoC assumes with each of the CoC-Approved programs.作者: 不幸的人 時間: 2025-3-24 11:32
0927-3042 ts. 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..978-1-4899-7890-5978-0-387-33225-3Series ISSN 0927-3042 Series E-ISSN 2509-8497 作者: 異教徒 時間: 2025-3-24 17:23 作者: outer-ear 時間: 2025-3-24 19:29
Ethical and Legal Issues in the Conduct of Cancer Clinical Trials, institution or academic medical center, the senior leadership at those institutions must demonstrate their commitment to establish and adequately fund regulatory compliance resources to assist and support physician investigators in this important and noble work.作者: 婚姻生活 時間: 2025-3-25 02:10 作者: 受傷 時間: 2025-3-25 03:45 作者: 任意 時間: 2025-3-25 10:27 作者: Integrate 時間: 2025-3-25 13:56 作者: landfill 時間: 2025-3-25 17:53 作者: 強有力 時間: 2025-3-25 21:03 作者: 謊言 時間: 2025-3-26 04:04
The Role of the FDA in Cancer Clinical Trials,ical investigator..The FDA has unique resources in terms of expertise and institutional experience, and has well defined mechanisms for interaction. Product development is viewed as a shared responsibility and the FDA can be an important and supportive partner in the process.作者: Defraud 時間: 2025-3-26 07:42
The Role of the FDA in Cancer Clinical Trials,uditing procedures, inspections, post marketing surveillance, safety analysis, preclinical data expectations, pharmacokinetics recommendations, Institutional Review Boards, Good Laboratory Practice, Good Manufacturing Practice, Good Clinical Practice and policy development have not been broached in 作者: Left-Atrium 時間: 2025-3-26 09:11 作者: Gourmet 時間: 2025-3-26 16:29
The Audit Process and How to Ensure a Successful Audit, malignancies. As an obligation to both the scientific community and the general public, the cooperative audit programs and the CTMB collaborate to ensure that the conduct of clinical trials are meticulous and the data are validated. However, audit programs should be viewed not merely as a surveilla作者: fibula 時間: 2025-3-26 18:48 作者: 朝圣者 時間: 2025-3-26 21:25
,The Commission on Cancer, American College of Surgeons’ Response to HIPAA,ch of the programs and the ACoS. Worrisome unintended consequences, potentially threatening the value of the products that the CoC provides cancer patients, providers, and families, were not realized because of the Business Associate role that the CoC assumes with each of the CoC-Approved programs.作者: poliosis 時間: 2025-3-27 02:25 作者: 違法事實 時間: 2025-3-27 07:25 作者: 小步舞 時間: 2025-3-27 10:26
The National Breast Cancer Coalition: Setting the Standard for Advocate Collaboration in Clinical T in the U.S. will die from the disease in 2005..These numbers will only decrease when prevention and a cure for the disease are found. Until then, the National Breast Cancer Coalition Fund will continue to bring the power of advocacy to influence science and industry in the pursuit of ending breast 作者: ethereal 時間: 2025-3-27 16:20 作者: ADOPT 時間: 2025-3-27 19:03 作者: 合唱隊 時間: 2025-3-27 23:34
,NCI’s Cancer Therapy Evaluation Program: A Commitment to Treatment Trials,作者: extrovert 時間: 2025-3-28 03:52
The Role of Cooperative Groups in Cancer Clinical Trials,作者: LATER 時間: 2025-3-28 09:39 作者: Kinetic 時間: 2025-3-28 12:21
The Role of the Office of Research Integrity in Cancer Clinical Trials,作者: Dawdle 時間: 2025-3-28 15:41 作者: Triglyceride 時間: 2025-3-28 22:32
The Clinical Research Process: Building a System in Harmony with its Users,作者: intoxicate 時間: 2025-3-29 00:26 作者: Kinetic 時間: 2025-3-29 04:41
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