Author: National Institutes of Health (U.S.)
Publisher:
ISBN:
Category : Government publications
Languages : en
Pages : 32
Book Description
A Guide to the NIH Research Contracting Process
Author: National Institutes of Health (U.S.)
Publisher:
ISBN:
Category : Government publications
Languages : en
Pages : 32
Book Description
Publisher:
ISBN:
Category : Government publications
Languages : en
Pages : 32
Book Description
A Guide to the NIH Research Contracting Process
Author:
Publisher:
ISBN:
Category : Public health
Languages : en
Pages : 25
Book Description
Publisher:
ISBN:
Category : Public health
Languages : en
Pages : 25
Book Description
A Guide to the NIH Research Contracting Process
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 25
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages : 25
Book Description
Guide to NIH Research Contracting Process
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 25
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages : 25
Book Description
NIH Guide for Grants and Contracts
Author:
Publisher:
ISBN:
Category : Medicine
Languages : en
Pages : 600
Book Description
Publisher:
ISBN:
Category : Medicine
Languages : en
Pages : 600
Book Description
The National Heart, Lung, and Blood Institute's Research Contracting Program
Author: National Heart, Lung, and Blood Institute. Contract Operations Branch
Publisher:
ISBN:
Category : Cardiovascular system
Languages : en
Pages : 16
Book Description
Publisher:
ISBN:
Category : Cardiovascular system
Languages : en
Pages : 16
Book Description
Research contracting program
Author: National Heart, Lung, and Blood Institute (U.S.).
Publisher:
ISBN:
Category :
Languages : en
Pages : 18
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages : 18
Book Description
Registries for Evaluating Patient Outcomes
Author: Agency for Healthcare Research and Quality/AHRQ
Publisher: Government Printing Office
ISBN: 1587634333
Category : Medical
Languages : en
Pages : 396
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.
Publisher: Government Printing Office
ISBN: 1587634333
Category : Medical
Languages : en
Pages : 396
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.
NCI Fact Book
Author: National Cancer Institute (U.S.)
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 82
Book Description
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 82
Book Description
Minority Access to Research Careers Program
Author:
Publisher:
ISBN:
Category : Medical personnel
Languages : en
Pages : 12
Book Description
Publisher:
ISBN:
Category : Medical personnel
Languages : en
Pages : 12
Book Description