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CORDIS FOCUS VOL. 180

CORDIS FOCUS VOL. 180 PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :

Book Description


CORDIS FOCUS VOL. 180

CORDIS FOCUS VOL. 180 PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :

Book Description


CORDIS FOCUS VOL. 182

CORDIS FOCUS VOL. 182 PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :

Book Description


CORDIS FOCUS VOL. 181

CORDIS FOCUS VOL. 181 PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :

Book Description


CORDIS FOCUS VOL. 183

CORDIS FOCUS VOL. 183 PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :

Book Description


09/01 CORDIS FOCUS VOL. 173

09/01 CORDIS FOCUS VOL. 173 PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :

Book Description


CORDIS Focus

CORDIS Focus PDF Author:
Publisher:
ISBN:
Category : Research
Languages : en
Pages : 160

Book Description


European Access

European Access PDF Author:
Publisher:
ISBN:
Category : European communities
Languages : en
Pages : 630

Book Description


Registries for Evaluating Patient Outcomes

Registries for Evaluating Patient Outcomes PDF Author: Agency for Healthcare Research and Quality/AHRQ
Publisher: Government Printing Office
ISBN: 1587634333
Category : Medical
Languages : en
Pages : 385

Book Description
This User’s Guide is intended to support the design, implementation, analysis, interpretation, and quality evaluation of registries created to increase understanding of patient outcomes. For the purposes of this guide, a patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves one or more predetermined scientific, clinical, or policy purposes. A registry database is a file (or files) derived from the registry. Although registries can serve many purposes, this guide focuses on registries created for one or more of the following purposes: to describe the natural history of disease, to determine clinical effectiveness or cost-effectiveness of health care products and services, to measure or monitor safety and harm, and/or to measure quality of care. Registries are classified according to how their populations are defined. For example, product registries include patients who have been exposed to biopharmaceutical products or medical devices. Health services registries consist of patients who have had a common procedure, clinical encounter, or hospitalization. Disease or condition registries are defined by patients having the same diagnosis, such as cystic fibrosis or heart failure. The User’s Guide was created by researchers affiliated with AHRQ’s Effective Health Care Program, particularly those who participated in AHRQ’s DEcIDE (Developing Evidence to Inform Decisions About Effectiveness) program. Chapters were subject to multiple internal and external independent reviews.

The Open Book of Social Innovation

The Open Book of Social Innovation PDF Author: Robin Murray
Publisher:
ISBN: 9781848750715
Category : Social change
Languages : en
Pages : 0

Book Description
"This book is about the many ways in which people are creating new and more effective answers to the biggest challenges of our times: how to cut our carbon footprint; how to keep people healthy; and how to end poverty. It describes the methods and tools for innovation being used across the world and across different sectors – the public and private sectors, civil society and the household – in the overlapping fields of the social economy, social entrepreneurship and social enterprise. It draws on inputs from hundreds of organisations to document the many methods currently being used around the world." -- Back cover.

Cochrane Handbook for Systematic Reviews of Interventions

Cochrane Handbook for Systematic Reviews of Interventions PDF Author: Julian P. T. Higgins
Publisher: Wiley
ISBN: 9780470699515
Category : Medical
Languages : en
Pages : 672

Book Description
Healthcare providers, consumers, researchers and policy makers are inundated with unmanageable amounts of information, including evidence from healthcare research. It has become impossible for all to have the time and resources to find, appraise and interpret this evidence and incorporate it into healthcare decisions. Cochrane Reviews respond to this challenge by identifying, appraising and synthesizing research-based evidence and presenting it in a standardized format, published in The Cochrane Library (www.thecochranelibrary.com). The Cochrane Handbook for Systematic Reviews of Interventions contains methodological guidance for the preparation and maintenance of Cochrane intervention reviews. Written in a clear and accessible format, it is the essential manual for all those preparing, maintaining and reading Cochrane reviews. Many of the principles and methods described here are appropriate for systematic reviews applied to other types of research and to systematic reviews of interventions undertaken by others. It is hoped therefore that this book will be invaluable to all those who want to understand the role of systematic reviews, critically appraise published reviews or perform reviews themselves.