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

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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

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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

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Sharing Clinical Trial Data

Sharing Clinical Trial Data PDF Author: Institute of Medicine
Publisher: National Academies Press
ISBN: 0309316324
Category : Medical
Languages : en
Pages : 304

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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 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

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Compilation of Cancer Therapy Protocol Summaries

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

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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.

Compilation of Clinical Protocol Summaries

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

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Book Description


Clinical Practice Guidelines We Can Trust

Clinical Practice Guidelines We Can Trust PDF Author: Institute of Medicine
Publisher: National Academies Press
ISBN: 030921646X
Category : Medical
Languages : en
Pages : 217

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Book Description
Advances in medical, biomedical and health services research have reduced the level of uncertainty in clinical practice. Clinical practice guidelines (CPGs) complement this progress by establishing standards of care backed by strong scientific evidence. CPGs are statements that include recommendations intended to optimize patient care. These statements are informed by a systematic review of evidence and an assessment of the benefits and costs of alternative care options. Clinical Practice Guidelines We Can Trust examines the current state of clinical practice guidelines and how they can be improved to enhance healthcare quality and patient outcomes. Clinical practice guidelines now are ubiquitous in our healthcare system. The Guidelines International Network (GIN) database currently lists more than 3,700 guidelines from 39 countries. Developing guidelines presents a number of challenges including lack of transparent methodological practices, difficulty reconciling conflicting guidelines, and conflicts of interest. Clinical Practice Guidelines We Can Trust explores questions surrounding the quality of CPG development processes and the establishment of standards. It proposes eight standards for developing trustworthy clinical practice guidelines emphasizing transparency; management of conflict of interest ; systematic review-guideline development intersection; establishing evidence foundations for and rating strength of guideline recommendations; articulation of recommendations; external review; and updating. Clinical Practice Guidelines We Can Trust shows how clinical practice guidelines can enhance clinician and patient decision-making by translating complex scientific research findings into recommendations for clinical practice that are relevant to the individual patient encounter, instead of implementing a one size fits all approach to patient care. This book contains information directly related to the work of the Agency for Healthcare Research and Quality (AHRQ), as well as various Congressional staff and policymakers. It is a vital resource for medical specialty societies, disease advocacy groups, health professionals, private and international organizations that develop or use clinical practice guidelines, consumers, clinicians, and payers.

Compilation of Experimental Cancer Therapy Protocol Summaries

Compilation of Experimental Cancer Therapy Protocol Summaries PDF Author:
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 740

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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

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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.

The National Cancer Program: Overview of program administration

The National Cancer Program: Overview of program administration PDF Author: United States. Congress. House. Committee on Government Operations. Intergovernmental Relations and Human Resources Subcommittee
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 866

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Book Description