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Compilation of Clinical Protocol Summaries

Compilation of Clinical Protocol Summaries PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :

Book Description


Compilation of Clinical Protocol Summaries

Compilation of Clinical Protocol Summaries PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :

Book Description


Compilation of Clinical Protocol Summaries

Compilation of Clinical Protocol Summaries PDF Author: Smithsonian Science Information Exchange. Current Cancer Research Project Analysis Center
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 412

Book Description


Compilation of Clinical Protocol Summaries

Compilation of Clinical Protocol Summaries PDF Author: International Cancer Research Data Bank
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 395

Book Description


Compilation of Clinical Protocol Summaries

Compilation of Clinical Protocol Summaries PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :

Book Description


Compilation of clinical protocol summaries

Compilation of clinical protocol summaries PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 578

Book Description


Sharing Clinical Trial Data

Sharing Clinical Trial Data PDF Author: Institute of Medicine
Publisher: National Academies Press
ISBN: 0309316324
Category : Medical
Languages : en
Pages : 236

Book Description
Data sharing can accelerate new discoveries by avoiding duplicative trials, stimulating new ideas for research, and enabling the maximal scientific knowledge and benefits to be gained from the efforts of clinical trial participants and investigators. At the same time, sharing clinical trial data presents risks, burdens, and challenges. These include the need to protect the privacy and honor the consent of clinical trial participants; safeguard the legitimate economic interests of sponsors; and guard against invalid secondary analyses, which could undermine trust in clinical trials or otherwise harm public health. Sharing Clinical Trial Data presents activities and strategies for the responsible sharing of clinical trial data. With the goal of increasing scientific knowledge to lead to better therapies for patients, this book identifies guiding principles and makes recommendations to maximize the benefits and minimize risks. This report offers guidance on the types of clinical trial data available at different points in the process, the points in the process at which each type of data should be shared, methods for sharing data, what groups should have access to data, and future knowledge and infrastructure needs. Responsible sharing of clinical trial data will allow other investigators to replicate published findings and carry out additional analyses, strengthen the evidence base for regulatory and clinical decisions, and increase the scientific knowledge gained from investments by the funders of clinical trials. The recommendations of Sharing Clinical Trial Data will be useful both now and well into the future as improved sharing of data leads to a stronger evidence base for treatment. This book will be of interest to stakeholders across the spectrum of research-from funders, to researchers, to journals, to physicians, and ultimately, to patients.

Compilation of Clinical Protocol Summaries

Compilation of Clinical Protocol Summaries PDF Author: Smithsonian Science Information Exchange
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 556

Book Description


Compilation of Cancer Therapy Protocol Summaries

Compilation of Cancer Therapy Protocol Summaries PDF Author: International Cancer Research Data Bank
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 764

Book Description


Compilation of Cancer Therapy Protocol Summaries

Compilation of Cancer Therapy Protocol Summaries PDF Author:
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 738

Book Description
Detailed outlines of ongoing experimental clinical trials. Data may also be retrieved in CLINPROT. Classified arrangement according to site. Each entry gives such information as investigator and address, objective, protocol outline, and dosage schedule. Tumor, agent, and protocol organizational number indexes. Miscellaneous appendixes.

Assuring Data Quality and Validity in Clinical Trials for Regulatory Decision Making

Assuring Data Quality and Validity in Clinical Trials for Regulatory Decision Making PDF Author: Institute of Medicine
Publisher: National Academies Press
ISBN: 0309172802
Category : Medical
Languages : en
Pages : 88

Book Description
In an effort to increase knowledge and understanding of the process of assuring data quality and validity in clinical trials, the IOM hosted a workshop to open a dialogue on the process to identify and discuss issues of mutual concern among industry, regulators, payers, and consumers. The presenters and panelists together developed strategies that could be used to address the issues that were identified. This IOM report of the workshop summarizes the present status and highlights possible strategies for making improvements to the education of interested and affected parties as well as facilitating future planning.